PubMed:15033202 / 835-968 JSONTXT

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    LitCoin-entities

    {"project":"LitCoin-entities","denotations":[{"id":"591","span":{"begin":19,"end":27},"obj":"OrganismTaxon"},{"id":"592","span":{"begin":123,"end":127},"obj":"GeneOrGeneProduct"}],"attributes":[{"id":"A18","pred":"db_id","subj":"591","obj":"NCBITaxon:9606"},{"id":"A19","pred":"db_id","subj":"592","obj":"NCBIGene:4683"}],"namespaces":[{"prefix":"_base","uri":"https://w3id.org/biolink/vocab/"},{"prefix":"MESH","uri":"http://id.nlm.nih.gov/mesh/"},{"prefix":"NCBITaxon","uri":"https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?id="},{"prefix":"NCBIGene","uri":"https://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"OMIM","uri":"https://www.omim.org/entry/"},{"prefix":"DBSNP","uri":"https://www.ncbi.nlm.nih.gov/snp/"}],"text":"We tested 67 Czech patients of different ages with simple microcephaly for the presence of the most common mutation in the NBS1 gene."}

    LitCoin-sentences

    {"project":"LitCoin-sentences","denotations":[{"id":"T7","span":{"begin":0,"end":133},"obj":"Sentence"}],"text":"We tested 67 Czech patients of different ages with simple microcephaly for the presence of the most common mutation in the NBS1 gene."}

    LitCoin_Mondo

    {"project":"LitCoin_Mondo","denotations":[{"id":"T12","span":{"begin":58,"end":70},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A12","pred":"mondo_id","subj":"T12","obj":"0001149"}],"text":"We tested 67 Czech patients of different ages with simple microcephaly for the presence of the most common mutation in the NBS1 gene."}

    LitCoin-GeneOrGeneProduct-v0

    {"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T20","span":{"begin":3,"end":9},"obj":"GeneOrGeneProduct"},{"id":"T21","span":{"begin":51,"end":57},"obj":"GeneOrGeneProduct"},{"id":"T22","span":{"begin":107,"end":115},"obj":"GeneOrGeneProduct"},{"id":"T23","span":{"begin":123,"end":127},"obj":"GeneOrGeneProduct"}],"text":"We tested 67 Czech patients of different ages with simple microcephaly for the presence of the most common mutation in the NBS1 gene."}

    LitCoin-GeneOrGeneProduct-v2

    {"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T16","span":{"begin":123,"end":127},"obj":"GeneOrGeneProduct"}],"text":"We tested 67 Czech patients of different ages with simple microcephaly for the presence of the most common mutation in the NBS1 gene."}

    LitCoin-Disease-MeSH

    {"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T13","span":{"begin":58,"end":70},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A13","pred":"originalLabel","subj":"T13","obj":"D008831"}],"text":"We tested 67 Czech patients of different ages with simple microcephaly for the presence of the most common mutation in the NBS1 gene."}

    LitCoin-GeneOrGeneProduct-v3

    {"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T7","span":{"begin":123,"end":127},"obj":"GeneOrGeneProduct"}],"text":"We tested 67 Czech patients of different ages with simple microcephaly for the presence of the most common mutation in the NBS1 gene."}

    LitCoin_Mondo_095

    {"project":"LitCoin_Mondo_095","denotations":[{"id":"T12","span":{"begin":58,"end":70},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A12","pred":"mondo_id","subj":"T12","obj":"0001149"}],"text":"We tested 67 Czech patients of different ages with simple microcephaly for the presence of the most common mutation in the NBS1 gene."}

    LitCoin-MeSH-Disease-2

    {"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T15","span":{"begin":58,"end":70},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A15","pred":"ID:","subj":"T15","obj":"D008831"}],"text":"We tested 67 Czech patients of different ages with simple microcephaly for the presence of the most common mutation in the NBS1 gene."}

    LitCoin-MONDO_bioort2019

    {"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T14","span":{"begin":58,"end":70},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A14","pred":"#label","subj":"T14","obj":"D008831"}],"text":"We tested 67 Czech patients of different ages with simple microcephaly for the presence of the most common mutation in the NBS1 gene."}

    LitCoin-NCBITaxon-2

    {"project":"LitCoin-NCBITaxon-2","denotations":[{"id":"T3","span":{"begin":19,"end":27},"obj":"OrganismTaxon"}],"text":"We tested 67 Czech patients of different ages with simple microcephaly for the presence of the most common mutation in the NBS1 gene."}

    LitCoin-training-merged

    {"project":"LitCoin-training-merged","denotations":[{"id":"T7","span":{"begin":123,"end":127},"obj":"GeneOrGeneProduct"},{"id":"T16923","span":{"begin":58,"end":70},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T18419","span":{"begin":19,"end":27},"obj":"OrganismTaxon"}],"attributes":[{"id":"A14","pred":"#label","subj":"T16923","obj":"D008831"}],"text":"We tested 67 Czech patients of different ages with simple microcephaly for the presence of the most common mutation in the NBS1 gene."}

    DisGeNET

    {"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":123,"end":127},"obj":"gene:4683"},{"id":"T1","span":{"begin":58,"end":70},"obj":"disease:C0025958"},{"id":"T2","span":{"begin":123,"end":127},"obj":"gene:55655"},{"id":"T3","span":{"begin":58,"end":70},"obj":"disease:C0025958"}],"relations":[{"id":"R1","pred":"associated_with","subj":"T0","obj":"T1"},{"id":"R2","pred":"associated_with","subj":"T2","obj":"T3"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"We tested 67 Czech patients of different ages with simple microcephaly for the presence of the most common mutation in the NBS1 gene."}