@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:NP382678.RAPm_pknRvVJ8thMD4XRDm-g5L7uvNnAfQVPc3B1Z0BwQ130_head { this: np:hasAssertion dgn-np:NP382678.RAPm_pknRvVJ8thMD4XRDm-g5L7uvNnAfQVPc3B1Z0BwQ130_assertion; np:hasProvenance dgn-np:NP382678.RAPm_pknRvVJ8thMD4XRDm-g5L7uvNnAfQVPc3B1Z0BwQ130_provenance; np:hasPublicationInfo dgn-np:NP382678.RAPm_pknRvVJ8thMD4XRDm-g5L7uvNnAfQVPc3B1Z0BwQ130_publicationInfo; a np:Nanopublication . dgn-np:NP382678.RAPm_pknRvVJ8thMD4XRDm-g5L7uvNnAfQVPc3B1Z0BwQ130_assertion a np:Assertion . dgn-np:NP382678.RAPm_pknRvVJ8thMD4XRDm-g5L7uvNnAfQVPc3B1Z0BwQ130_provenance a np:Provenance . dgn-np:NP382678.RAPm_pknRvVJ8thMD4XRDm-g5L7uvNnAfQVPc3B1Z0BwQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP382678.RAPm_pknRvVJ8thMD4XRDm-g5L7uvNnAfQVPc3B1Z0BwQ130_assertion { miriam-gene:2073 a ncit:C16612 . lld:C0009207 a ncit:C7057 . dgn-gda:DGN077467e2628a7c2dacae8dd269279cfa sio:SIO_000628 miriam-gene:2073, lld:C0009207; a sio:SIO_001121 . } dgn-np:NP382678.RAPm_pknRvVJ8thMD4XRDm-g5L7uvNnAfQVPc3B1Z0BwQ130_provenance { dgn-np:NP382678.RAPm_pknRvVJ8thMD4XRDm-g5L7uvNnAfQVPc3B1Z0BwQ130_assertion dcterms:description "[Primary cells from patients have been instrumental to elucidate the multiple roles of CS proteins and to approach the dissection of the complex interplay between repair and transcription that is central to the CS clinical phenotype.]. 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:23567079; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP382678.RAPm_pknRvVJ8thMD4XRDm-g5L7uvNnAfQVPc3B1Z0BwQ130_publicationInfo { this: dcterms:created "2015-08-25T14:41:21+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" . }