@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:NP53655.RATWn2HLogasFYfTa36sb-VvVrPA4t1mO1zZRnDbYQhfI130_head { this: np:hasAssertion dgn-np:NP53655.RATWn2HLogasFYfTa36sb-VvVrPA4t1mO1zZRnDbYQhfI130_assertion; np:hasProvenance dgn-np:NP53655.RATWn2HLogasFYfTa36sb-VvVrPA4t1mO1zZRnDbYQhfI130_provenance; np:hasPublicationInfo dgn-np:NP53655.RATWn2HLogasFYfTa36sb-VvVrPA4t1mO1zZRnDbYQhfI130_publicationInfo; a np:Nanopublication . dgn-np:NP53655.RATWn2HLogasFYfTa36sb-VvVrPA4t1mO1zZRnDbYQhfI130_assertion a np:Assertion . dgn-np:NP53655.RATWn2HLogasFYfTa36sb-VvVrPA4t1mO1zZRnDbYQhfI130_provenance a np:Provenance . dgn-np:NP53655.RATWn2HLogasFYfTa36sb-VvVrPA4t1mO1zZRnDbYQhfI130_publicationInfo a np:PublicationInfo . } dgn-np:NP53655.RATWn2HLogasFYfTa36sb-VvVrPA4t1mO1zZRnDbYQhfI130_assertion { miriam-gene:100048912 a ncit:C16612 . lld:C0007766 a ncit:C7057 . dgn-gda:DGN70dff942f56af3376e9c1ab87639d528 sio:SIO_000628 miriam-gene:100048912, lld:C0007766; a sio:SIO_001122 . } dgn-np:NP53655.RATWn2HLogasFYfTa36sb-VvVrPA4t1mO1zZRnDbYQhfI130_provenance { dgn-np:NP53655.RATWn2HLogasFYfTa36sb-VvVrPA4t1mO1zZRnDbYQhfI130_assertion dcterms:description "[However, the metaanalysis yielded genomewide significance for SNP on chromosome 9p (CDKN2BAS; rs6475606; P=3.6×10(-8)) and provided further evidence to support the previously reported association of IA with SNP in SOX17 on chromosome 8q (rs1072737; P=8.7×10(-5)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_curated; sio:SIO_000772 miriam-pubmed:22961961; prov:wasDerivedFrom dgn-void:gwascat-2016; prov:wasGeneratedBy eco:ECO_0000218 . dgn-void:gwascat-2016 pav:importedOn "2016-01-27"^^xsd:date . dgn-void:source_evidence_curated a eco:ECO_0000205; rdfs:comment "Gene-disease associations manually curated."@en; rdfs:label "DisGeNET evidence - CURATED"@en . } dgn-np:NP53655.RATWn2HLogasFYfTa36sb-VvVrPA4t1mO1zZRnDbYQhfI130_publicationInfo { this: dcterms:created "2016-05-13T12:42:12+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" . }