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PubMed:15099351 JSONTXT 12 Projects

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Id Subject Object Predicate Lexical cue #label ID:
T29252 17-22 GeneOrGeneProduct denotes PCSK9
T1 55-94 DiseaseOrPhenotypicFeature denotes autosomal dominant hypercholesterolemia D006938
T64234 74-94 GeneOrGeneProduct denotes hypercholesterolemia
T50226 96-139 GeneOrGeneProduct denotes Proprotein convertase subtilisin/kexin type
T47892 96-141 ChemicalEntity denotes Proprotein convertase subtilisin/kexin type 9 D000071449
T85471 143-148 GeneOrGeneProduct denotes PCSK9
T2 168-207 DiseaseOrPhenotypicFeature denotes autosomal dominant hypercholesterolemia D006938
T7959 187-207 GeneOrGeneProduct denotes hypercholesterolemia
T42813 243-248 GeneOrGeneProduct denotes PCSK9
T86888 269-280 ChemicalEntity denotes cholesterol D002784|http://purl.obolibrary.org/obo/CHEBI_16113
T7 367-387 GeneOrGeneProduct denotes hypercholesterolemia
T3 367-387 DiseaseOrPhenotypicFeature denotes hypercholesterolemia D006937
T8 442-447 GeneOrGeneProduct denotes PCSK9
T4 526-555 DiseaseOrPhenotypicFeature denotes familial hypercholesterolemia D006938
T9 535-555 GeneOrGeneProduct denotes hypercholesterolemia
T89948 579-602 ChemicalEntity denotes low-density lipoprotein http://purl.obolibrary.org/obo/CHEBI_39026
T10 579-611 GeneOrGeneProduct denotes low-density lipoprotein receptor
T35421 630-636 SequenceVariant denotes R3500Q
T84945 644-658 ChemicalEntity denotes apolipoprotein http://purl.obolibrary.org/obo/CHEBI_39015
T11 644-664 GeneOrGeneProduct denotes apolipoprotein B-100
T12 766-771 GeneOrGeneProduct denotes PCSK9
T59437 782-790 OrganismTaxon denotes patients
T30216 814-819 SequenceVariant denotes D374Y
T77087 829-836 OrganismTaxon denotes patient
T9278 867-872 SequenceVariant denotes D374Y
T99890 877-882 SequenceVariant denotes N157K
T66898 884-889 SequenceVariant denotes D374Y
T13 906-926 GeneOrGeneProduct denotes hypercholesterolemia
T5 906-926 DiseaseOrPhenotypicFeature denotes hypercholesterolemia D006937
T14 1055-1060 GeneOrGeneProduct denotes PCSK9
T6 1072-1111 DiseaseOrPhenotypicFeature denotes autosomal dominant hypercholesterolemia D006938
T15 1091-1111 GeneOrGeneProduct denotes hypercholesterolemia