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PubMed:10024240 JSONTXT

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bionlp-st-gro-2013-development

Id Subject Object Predicate Lexical cue
T1 50-55 Eukaryote denotes human
T2 56-63 Tissue denotes cardiac
T3 68-80 Tissue denotes craniofacial
T4 108-118 Chromosome denotes chromosome
T5 177-184 Tissue denotes cardiac
T6 189-201 Tissue denotes craniofacial
T7 215-221 Eukaryote denotes humans
T8 236-241 Eukaryote denotes mouse
T9 242-247 Gene denotes genes
T10 261-266 TranscriptionFactor denotes dHAND
T11 270-290 TranscriptionFactor denotes transcription factor
T13 342-346 Gene denotes Ufd1
T14 362-367 Eukaryote denotes human
T15 388-395 Protein denotes protein
T18 447-452 Eukaryote denotes Mouse
T19 453-457 Protein denotes Ufd1
T21 493-500 Tissue denotes tissues
T23 556-561 Eukaryote denotes human
T24 562-572 Gene denotes UFD1L gene
T25 700-705 Exon denotes exons
T26 716-721 Gene denotes UFD1L
T27 824-829 Gene denotes UFD1L
T30 305-317 Tissue denotes neural crest
T31 368-373 Chromosome denotes 22q11
T17 437-445 Protein denotes proteins
T22 527-532 Chromosome denotes 22q11
T36 618-623 Chromosome denotes 22q11
T38 775-780 Chromosome denotes 22q11
T41 879-884 Tissue denotes heart
T42 889-901 Tissue denotes craniofacial
T43 918-923 Chromosome denotes 22q11
E2 408-419 ProteinCatabolism denotes degradation
E3 475-484 GeneExpression denotes expressed
E5 12-19 Pathway denotes pathway
E6 90-104 Mutation denotes Microdeletions
E1 318-329 DevelopmentalProcess denotes development
E7 423-436 ProteinModification denotes ubiquitinated
E4 533-541 Mutation denotes deletion
E8 542-550 Disease denotes syndrome
E9 577-584 Mutation denotes deleted
E10 624-632 Mutation denotes deletion
E11 781-789 Mutation denotes deletion
E12 790-798 Disease denotes syndrome
E13 924-932 Mutation denotes deletion
R1 T2 T1 fromSpecies cardiac,human
R2 T3 T1 fromSpecies craniofacial,human
R3 T5 T7 fromSpecies cardiac,humans
R4 T6 T7 fromSpecies craniofacial,humans
R5 T9 T8 fromSpecies genes,mouse
R6 T13 T15 encodes Ufd1,protein
R8 T19 T18 fromSpecies Ufd1,Mouse
R9 E3 T21 locatedIn expressed,tissues
R10 T24 T23 fromSpecies UFD1L gene,human
R11 T26 T25 hasPart UFD1L,exons
R12 E6 T4 locatedIn Microdeletions,chromosome
R13 T13 T31 locatedIn Ufd1,22q11
R7 T31 T14 fromSpecies 22q11,human
R14 E4 T22 locatedIn deletion,22q11
R15 E10 T36 locatedIn deletion,22q11
R16 E11 T38 locatedIn deletion,22q11
R17 E13 T43 locatedIn deletion,22q11
R19 T17 E2 hasPatient proteins,degradation
R20 T19 E3 hasPatient Ufd1,expressed
R21 T11 E1 hasAgent transcription factor,development
R22 T30 E1 hasPatient neural crest,development
R23 T17 E7 hasPatient proteins,ubiquitinated
R24 T24 E9 hasPatient UFD1L gene,deleted

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 177-211 HP_0001627 denotes cardiac and craniofacial anomalies
T2 189-211 HP_0001999 denotes craniofacial anomalies
T3 868-909 HP_0002564 denotes congenital heart and craniofacial defects
T4 879-909 HP_0001627 denotes heart and craniofacial defects
T5 889-909 HP_0001999 denotes craniofacial defects

DisGeNET

Id Subject Object Predicate Lexical cue
T0 453-457 gene:7353 denotes Ufd1
T1 527-550 disease:C2936346 denotes 22q11 deletion syndrome
T2 716-721 gene:7353 denotes UFD1L
T3 775-798 disease:C2936346 denotes 22q11 deletion syndrome
T4 562-567 gene:7353 denotes UFD1L
T5 775-798 disease:C2936346 denotes 22q11 deletion syndrome
R1 T0 T1 associated_with Ufd1,22q11 deletion syndrome
R2 T2 T3 associated_with UFD1L,22q11 deletion syndrome
R3 T4 T5 associated_with UFD1L,22q11 deletion syndrome

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10024240-4#10#15#gene7353 562-567 gene7353 denotes UFD1L
10024240-4#164#169#gene7353 716-721 gene7353 denotes UFD1L
10024240-4#223#246#diseaseC2936346 775-798 diseaseC2936346 denotes 22q11 deletion syndrome
10#15#gene7353223#246#diseaseC2936346 10024240-4#10#15#gene7353 10024240-4#223#246#diseaseC2936346 associated_with UFD1L,22q11 deletion syndrome
164#169#gene7353223#246#diseaseC2936346 10024240-4#164#169#gene7353 10024240-4#223#246#diseaseC2936346 associated_with UFD1L,22q11 deletion syndrome