@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:NP1365012.RAtt0Bo7jAIL3a32dyMlsjDixC8NdpSrlBCb5CIBnc19s130_head { this: np:hasAssertion dgn-np:NP1365012.RAtt0Bo7jAIL3a32dyMlsjDixC8NdpSrlBCb5CIBnc19s130_assertion; np:hasProvenance dgn-np:NP1365012.RAtt0Bo7jAIL3a32dyMlsjDixC8NdpSrlBCb5CIBnc19s130_provenance; np:hasPublicationInfo dgn-np:NP1365012.RAtt0Bo7jAIL3a32dyMlsjDixC8NdpSrlBCb5CIBnc19s130_publicationInfo; a np:Nanopublication . dgn-np:NP1365012.RAtt0Bo7jAIL3a32dyMlsjDixC8NdpSrlBCb5CIBnc19s130_assertion a np:Assertion . dgn-np:NP1365012.RAtt0Bo7jAIL3a32dyMlsjDixC8NdpSrlBCb5CIBnc19s130_provenance a np:Provenance . dgn-np:NP1365012.RAtt0Bo7jAIL3a32dyMlsjDixC8NdpSrlBCb5CIBnc19s130_publicationInfo a np:PublicationInfo . } dgn-np:NP1365012.RAtt0Bo7jAIL3a32dyMlsjDixC8NdpSrlBCb5CIBnc19s130_assertion { miriam-gene:2966 a ncit:C16612 . lld:C0026847 a ncit:C7057 . dgn-gda:DGNc6160bfe50f4eddc58948014afdca997 sio:SIO_000628 miriam-gene:2966, lld:C0026847; a sio:SIO_001121 . } dgn-np:NP1365012.RAtt0Bo7jAIL3a32dyMlsjDixC8NdpSrlBCb5CIBnc19s130_provenance { dgn-np:NP1365012.RAtt0Bo7jAIL3a32dyMlsjDixC8NdpSrlBCb5CIBnc19s130_assertion dcterms:description "[The TFIIH polypeptide composition as well as transcription and DNA repair activities are normal in patients lacking the p44t gene on both mutant chromosomes, suggesting that the p44t gene is not critical for the development of SMA.]. 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:8981949; 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:NP1365012.RAtt0Bo7jAIL3a32dyMlsjDixC8NdpSrlBCb5CIBnc19s130_publicationInfo { this: dcterms:created "2016-05-13T12:52:04+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" . }