@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:NP992325.RA88Kfr1K9uL3vf0vohJcCoZCJOtc2z4hL5nXjX4QrZTQ130_head { this: np:hasAssertion dgn-np:NP992325.RA88Kfr1K9uL3vf0vohJcCoZCJOtc2z4hL5nXjX4QrZTQ130_assertion; np:hasProvenance dgn-np:NP992325.RA88Kfr1K9uL3vf0vohJcCoZCJOtc2z4hL5nXjX4QrZTQ130_provenance; np:hasPublicationInfo dgn-np:NP992325.RA88Kfr1K9uL3vf0vohJcCoZCJOtc2z4hL5nXjX4QrZTQ130_publicationInfo; a np:Nanopublication . dgn-np:NP992325.RA88Kfr1K9uL3vf0vohJcCoZCJOtc2z4hL5nXjX4QrZTQ130_assertion a np:Assertion . dgn-np:NP992325.RA88Kfr1K9uL3vf0vohJcCoZCJOtc2z4hL5nXjX4QrZTQ130_provenance a np:Provenance . dgn-np:NP992325.RA88Kfr1K9uL3vf0vohJcCoZCJOtc2z4hL5nXjX4QrZTQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP992325.RA88Kfr1K9uL3vf0vohJcCoZCJOtc2z4hL5nXjX4QrZTQ130_assertion { miriam-gene:79728 a ncit:C16612 . lld:C0678222 a ncit:C7057 . dgn-gda:DGN42e197833267f949d4fb1e6e58afd9df sio:SIO_000628 miriam-gene:79728, lld:C0678222; a sio:SIO_001121 . } dgn-np:NP992325.RA88Kfr1K9uL3vf0vohJcCoZCJOtc2z4hL5nXjX4QrZTQ130_provenance { dgn-np:NP992325.RA88Kfr1K9uL3vf0vohJcCoZCJOtc2z4hL5nXjX4QrZTQ130_assertion dcterms:description "[Deleterious mutations in few genes involved in the Fanconi complex are responsible for Fanconi anemia at the homozygous state and breast cancer (BC) susceptibility at the heterozygous state (BRCA2, PALB2, BRIP1).]. 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:22725699; 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:NP992325.RA88Kfr1K9uL3vf0vohJcCoZCJOtc2z4hL5nXjX4QrZTQ130_publicationInfo { this: dcterms:created "2016-05-13T12:49:15+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" . }