@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:NP740806.RA7NqcFtlKqp2JBUKiwEnCz2aK2E-2r9MPPjxxXDsEgis130_head { this: np:hasAssertion dgn-np:NP740806.RA7NqcFtlKqp2JBUKiwEnCz2aK2E-2r9MPPjxxXDsEgis130_assertion; np:hasProvenance dgn-np:NP740806.RA7NqcFtlKqp2JBUKiwEnCz2aK2E-2r9MPPjxxXDsEgis130_provenance; np:hasPublicationInfo dgn-np:NP740806.RA7NqcFtlKqp2JBUKiwEnCz2aK2E-2r9MPPjxxXDsEgis130_publicationInfo; a np:Nanopublication . dgn-np:NP740806.RA7NqcFtlKqp2JBUKiwEnCz2aK2E-2r9MPPjxxXDsEgis130_assertion a np:Assertion . dgn-np:NP740806.RA7NqcFtlKqp2JBUKiwEnCz2aK2E-2r9MPPjxxXDsEgis130_provenance a np:Provenance . dgn-np:NP740806.RA7NqcFtlKqp2JBUKiwEnCz2aK2E-2r9MPPjxxXDsEgis130_publicationInfo a np:PublicationInfo . } dgn-np:NP740806.RA7NqcFtlKqp2JBUKiwEnCz2aK2E-2r9MPPjxxXDsEgis130_assertion { miriam-gene:641 a ncit:C16612 . lld:C0015625 a ncit:C7057 . dgn-gda:DGNb9016284785b6fed74e07cd4b132498a sio:SIO_000628 miriam-gene:641, lld:C0015625; a sio:SIO_001121 . } dgn-np:NP740806.RA7NqcFtlKqp2JBUKiwEnCz2aK2E-2r9MPPjxxXDsEgis130_provenance { dgn-np:NP740806.RA7NqcFtlKqp2JBUKiwEnCz2aK2E-2r9MPPjxxXDsEgis130_assertion dcterms:description "[The products of the 13 FANC genes (mutated in Fanconi anaemia), which constitute the 'FANC' pathway, and BLM (the RecQ helicase mutated in Bloom syndrome) are thought to collaborate during the S phase of the cell cycle, preventing chromosome instability.]. 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:19465921; 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:NP740806.RA7NqcFtlKqp2JBUKiwEnCz2aK2E-2r9MPPjxxXDsEgis130_publicationInfo { this: dcterms:created "2016-05-13T12:47:21+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 "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }