@prefix bfo: . @prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP237396.RAJcEgXgDUFvuCY5yoqum6nZPRvZWdKa60e9Ovz5onOlA130_head { this: np:hasAssertion dgn-np:NP237396.RAJcEgXgDUFvuCY5yoqum6nZPRvZWdKa60e9Ovz5onOlA130_assertion; np:hasProvenance dgn-np:NP237396.RAJcEgXgDUFvuCY5yoqum6nZPRvZWdKa60e9Ovz5onOlA130_provenance; np:hasPublicationInfo dgn-np:NP237396.RAJcEgXgDUFvuCY5yoqum6nZPRvZWdKa60e9Ovz5onOlA130_publicationInfo; a np:Nanopublication . dgn-np:NP237396.RAJcEgXgDUFvuCY5yoqum6nZPRvZWdKa60e9Ovz5onOlA130_assertion a np:Assertion . dgn-np:NP237396.RAJcEgXgDUFvuCY5yoqum6nZPRvZWdKa60e9Ovz5onOlA130_provenance a np:Provenance . dgn-np:NP237396.RAJcEgXgDUFvuCY5yoqum6nZPRvZWdKa60e9Ovz5onOlA130_publicationInfo a np:PublicationInfo . } dgn-np:NP237396.RAJcEgXgDUFvuCY5yoqum6nZPRvZWdKa60e9Ovz5onOlA130_assertion { miriam-gene:6910 a ncit:C16612 . lld:C0018799 a ncit:C7057 . dgn-gda:DGN8d8f1a16b10a1d4aaabb2df8e6f5a91d sio:SIO_000628 miriam-gene:6910, lld:C0018799; a sio:SIO_001121 . } dgn-np:NP237396.RAJcEgXgDUFvuCY5yoqum6nZPRvZWdKa60e9Ovz5onOlA130_provenance { dgn-np:NP237396.RAJcEgXgDUFvuCY5yoqum6nZPRvZWdKa60e9Ovz5onOlA130_assertion dcterms:description "[we describe a large atypical Holt-Oram syndrome family with mild skeletal deformations and paroxysmal atrial fibrillation, but few have congenital heart disease/of TBX5 revealed a novel mutation, c.373G > A, resulting in p.Gly125Arg.]. 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:18451335; prov:wasDerivedFrom dgn-void:lhgdn-20090331; prov:wasGeneratedBy bfo:ECO_0000203 . dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^xsd:date . dgn-void:source_evidence_literature a bfo:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP237396.RAJcEgXgDUFvuCY5yoqum6nZPRvZWdKa60e9Ovz5onOlA130_publicationInfo { this: dcterms:created "2016-05-13T12:43:33+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" . }