@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:NP852482.RA2lWxomLMQwu3a3ObTtYffl5SWCW4-Q_EkxjEKkFn1JU130_head { this: np:hasAssertion dgn-np:NP852482.RA2lWxomLMQwu3a3ObTtYffl5SWCW4-Q_EkxjEKkFn1JU130_assertion; np:hasProvenance dgn-np:NP852482.RA2lWxomLMQwu3a3ObTtYffl5SWCW4-Q_EkxjEKkFn1JU130_provenance; np:hasPublicationInfo dgn-np:NP852482.RA2lWxomLMQwu3a3ObTtYffl5SWCW4-Q_EkxjEKkFn1JU130_publicationInfo; a np:Nanopublication . dgn-np:NP852482.RA2lWxomLMQwu3a3ObTtYffl5SWCW4-Q_EkxjEKkFn1JU130_assertion a np:Assertion . dgn-np:NP852482.RA2lWxomLMQwu3a3ObTtYffl5SWCW4-Q_EkxjEKkFn1JU130_provenance a np:Provenance . dgn-np:NP852482.RA2lWxomLMQwu3a3ObTtYffl5SWCW4-Q_EkxjEKkFn1JU130_publicationInfo a np:PublicationInfo . } dgn-np:NP852482.RA2lWxomLMQwu3a3ObTtYffl5SWCW4-Q_EkxjEKkFn1JU130_assertion { miriam-gene:10752 a ncit:C16612 . lld:C1306459 a ncit:C7057 . dgn-gda:DGN3c87c45f2a389061ee993226557547a8 sio:SIO_000628 miriam-gene:10752, lld:C1306459; a sio:SIO_001121 . } dgn-np:NP852482.RA2lWxomLMQwu3a3ObTtYffl5SWCW4-Q_EkxjEKkFn1JU130_provenance { dgn-np:NP852482.RA2lWxomLMQwu3a3ObTtYffl5SWCW4-Q_EkxjEKkFn1JU130_assertion dcterms:description "[Together, the sequence variations provide MHH-CALL-2 with capabilities typically acquired during cancer development, e.g., loss of cell cycle control, enhanced proliferation, lack of DNA repair, cell death evasion, and disturbance of epigenetic gene regulation.]. 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:23508829; 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:NP852482.RA2lWxomLMQwu3a3ObTtYffl5SWCW4-Q_EkxjEKkFn1JU130_publicationInfo { this: dcterms:created "2015-08-25T14:46:17+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" . }