@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:NP106575.RAszw1ZqrF5CnFtv8o5BhEnwHI61EU_5rBvysB8hyC1Q4130_head { this: np:hasAssertion dgn-np:NP106575.RAszw1ZqrF5CnFtv8o5BhEnwHI61EU_5rBvysB8hyC1Q4130_assertion; np:hasProvenance dgn-np:NP106575.RAszw1ZqrF5CnFtv8o5BhEnwHI61EU_5rBvysB8hyC1Q4130_provenance; np:hasPublicationInfo dgn-np:NP106575.RAszw1ZqrF5CnFtv8o5BhEnwHI61EU_5rBvysB8hyC1Q4130_publicationInfo; a np:Nanopublication . dgn-np:NP106575.RAszw1ZqrF5CnFtv8o5BhEnwHI61EU_5rBvysB8hyC1Q4130_assertion a np:Assertion . dgn-np:NP106575.RAszw1ZqrF5CnFtv8o5BhEnwHI61EU_5rBvysB8hyC1Q4130_provenance a np:Provenance . dgn-np:NP106575.RAszw1ZqrF5CnFtv8o5BhEnwHI61EU_5rBvysB8hyC1Q4130_publicationInfo a np:PublicationInfo . } dgn-np:NP106575.RAszw1ZqrF5CnFtv8o5BhEnwHI61EU_5rBvysB8hyC1Q4130_assertion { miriam-gene:2626 a ncit:C16612 . lld:C0039685 a ncit:C7057 . dgn-gda:DGN4a932615533942be7a256f399f9d7f6f sio:SIO_000628 miriam-gene:2626, lld:C0039685; a sio:SIO_001122 . } dgn-np:NP106575.RAszw1ZqrF5CnFtv8o5BhEnwHI61EU_5rBvysB8hyC1Q4130_provenance { dgn-np:NP106575.RAszw1ZqrF5CnFtv8o5BhEnwHI61EU_5rBvysB8hyC1Q4130_assertion dcterms:description "[We analysed the GATA binding protein 4 gene, or GATA4, along with the NK2 transcription factor related, locus 5 gene, or NKX2.5, to determine their genetic contribution to 104 sporadic patients in Indonesia with congenitally malformed hearts, 76 cases having atrial septal defect and 28 tetralogy of Fallot.]. 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:19678963; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP106575.RAszw1ZqrF5CnFtv8o5BhEnwHI61EU_5rBvysB8hyC1Q4130_publicationInfo { this: dcterms:created "2015-08-25T14:38:39+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }