@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:NP1201826.RAidui8WwDET8WZ1ej8il6K7KhaJtQ21_0DdQ3pfdAT-E130_head { this: np:hasAssertion dgn-np:NP1201826.RAidui8WwDET8WZ1ej8il6K7KhaJtQ21_0DdQ3pfdAT-E130_assertion; np:hasProvenance dgn-np:NP1201826.RAidui8WwDET8WZ1ej8il6K7KhaJtQ21_0DdQ3pfdAT-E130_provenance; np:hasPublicationInfo dgn-np:NP1201826.RAidui8WwDET8WZ1ej8il6K7KhaJtQ21_0DdQ3pfdAT-E130_publicationInfo; a np:Nanopublication . dgn-np:NP1201826.RAidui8WwDET8WZ1ej8il6K7KhaJtQ21_0DdQ3pfdAT-E130_assertion a np:Assertion . dgn-np:NP1201826.RAidui8WwDET8WZ1ej8il6K7KhaJtQ21_0DdQ3pfdAT-E130_provenance a np:Provenance . dgn-np:NP1201826.RAidui8WwDET8WZ1ej8il6K7KhaJtQ21_0DdQ3pfdAT-E130_publicationInfo a np:PublicationInfo . } dgn-np:NP1201826.RAidui8WwDET8WZ1ej8il6K7KhaJtQ21_0DdQ3pfdAT-E130_assertion { miriam-gene:1482 a ncit:C16612 . lld:C1389018 a ncit:C7057 . dgn-gda:DGN1eea7b06b2eb351aeb5d69a35cd61d35 sio:SIO_000628 miriam-gene:1482, lld:C1389018; a sio:SIO_001122 . } dgn-np:NP1201826.RAidui8WwDET8WZ1ej8il6K7KhaJtQ21_0DdQ3pfdAT-E130_provenance { dgn-np:NP1201826.RAidui8WwDET8WZ1ej8il6K7KhaJtQ21_0DdQ3pfdAT-E130_assertion dcterms:description "[All the heterozygous neonatal Nkx2-5(+/R52G) mice demonstrated a prominent trabecular layer in the ventricular wall, so called noncompaction, along with diverse cardiac anomalies, including atrioventricular septal defects, Ebstein malformation of the tricuspid valve, and perimembranous and muscular ventricular septal defects.]. 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:25028484; 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:NP1201826.RAidui8WwDET8WZ1ej8il6K7KhaJtQ21_0DdQ3pfdAT-E130_publicationInfo { this: dcterms:created "2016-05-13T12:50:50+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" . }