@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:NP1387890.RAW_o65Py8RHbQ5ULjnrvTCRhAk2GWLpEpmkBNsOIMayI130_head { this: np:hasAssertion dgn-np:NP1387890.RAW_o65Py8RHbQ5ULjnrvTCRhAk2GWLpEpmkBNsOIMayI130_assertion; np:hasProvenance dgn-np:NP1387890.RAW_o65Py8RHbQ5ULjnrvTCRhAk2GWLpEpmkBNsOIMayI130_provenance; np:hasPublicationInfo dgn-np:NP1387890.RAW_o65Py8RHbQ5ULjnrvTCRhAk2GWLpEpmkBNsOIMayI130_publicationInfo; a np:Nanopublication . dgn-np:NP1387890.RAW_o65Py8RHbQ5ULjnrvTCRhAk2GWLpEpmkBNsOIMayI130_assertion a np:Assertion . dgn-np:NP1387890.RAW_o65Py8RHbQ5ULjnrvTCRhAk2GWLpEpmkBNsOIMayI130_provenance a np:Provenance . dgn-np:NP1387890.RAW_o65Py8RHbQ5ULjnrvTCRhAk2GWLpEpmkBNsOIMayI130_publicationInfo a np:PublicationInfo . } dgn-np:NP1387890.RAW_o65Py8RHbQ5ULjnrvTCRhAk2GWLpEpmkBNsOIMayI130_assertion { miriam-gene:6899 a ncit:C16612 . lld:C0220704 a ncit:C7057 . dgn-gda:DGN02ba2593d19aaaf6724c64dcad210f3f sio:SIO_000628 miriam-gene:6899, lld:C0220704; a sio:SIO_001121 . } dgn-np:NP1387890.RAW_o65Py8RHbQ5ULjnrvTCRhAk2GWLpEpmkBNsOIMayI130_provenance { dgn-np:NP1387890.RAW_o65Py8RHbQ5ULjnrvTCRhAk2GWLpEpmkBNsOIMayI130_assertion dcterms:description "[Here we demonstrate that mice deficient for one type of endothelin receptor, ETA, mimic the human conditions collectively termed CATCH 22 or velocardiofacial syndrome, which include severe craniofacial deformities and defects in the cardiovascular outflow tract.]. 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:9449664; 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:NP1387890.RAW_o65Py8RHbQ5ULjnrvTCRhAk2GWLpEpmkBNsOIMayI130_publicationInfo { this: dcterms:created "2016-05-13T12:52:15+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" . }