@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP779052.RAAgLFQUB9gurwNz_tkHR80yaweiL0MdUlluYO2LHIbKQ130_head { this: np:hasAssertion dgn-np:NP779052.RAAgLFQUB9gurwNz_tkHR80yaweiL0MdUlluYO2LHIbKQ130_assertion; np:hasProvenance dgn-np:NP779052.RAAgLFQUB9gurwNz_tkHR80yaweiL0MdUlluYO2LHIbKQ130_provenance; np:hasPublicationInfo dgn-np:NP779052.RAAgLFQUB9gurwNz_tkHR80yaweiL0MdUlluYO2LHIbKQ130_publicationInfo; a np:Nanopublication . dgn-np:NP779052.RAAgLFQUB9gurwNz_tkHR80yaweiL0MdUlluYO2LHIbKQ130_assertion a np:Assertion . dgn-np:NP779052.RAAgLFQUB9gurwNz_tkHR80yaweiL0MdUlluYO2LHIbKQ130_provenance a np:Provenance . dgn-np:NP779052.RAAgLFQUB9gurwNz_tkHR80yaweiL0MdUlluYO2LHIbKQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP779052.RAAgLFQUB9gurwNz_tkHR80yaweiL0MdUlluYO2LHIbKQ130_assertion { miriam-gene:50943 a ncit:C16612 . lld:C0011854 a ncit:C7057 . dgn-gda:DGNa35d1bd349fbca838679672d757533ed sio:SIO_000628 miriam-gene:50943, lld:C0011854; a sio:SIO_001121 . } dgn-np:NP779052.RAAgLFQUB9gurwNz_tkHR80yaweiL0MdUlluYO2LHIbKQ130_provenance { dgn-np:NP779052.RAAgLFQUB9gurwNz_tkHR80yaweiL0MdUlluYO2LHIbKQ130_assertion dcterms:description "[Here, 257 single-nucleotide polymorphisms (SNPs) have been genotyped in 19 candidate genes (INS, PTPN22, IL2RA, CTLA4, IFIH1, SUMO4, VDR, PAX4, OAS1, IRS1, IL4, IL4R, IL13, IL12B, CEACAM21, CAPSL, Q7Z4c4(5Q), FOXP3, EFHB) in 2300 affected sib-pair families and tested for association with T1D as part of the Type I Diabetes Genetics Consortium's candidate gene study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:19956106; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP779052.RAAgLFQUB9gurwNz_tkHR80yaweiL0MdUlluYO2LHIbKQ130_publicationInfo { this: dcterms:created "2016-05-13T12:47:38+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }