@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:NP318066.RApURtsBnWbBT49j8ZFe5jf4If0gUyeSXo_073jetWXxY130_head { this: np:hasAssertion dgn-np:NP318066.RApURtsBnWbBT49j8ZFe5jf4If0gUyeSXo_073jetWXxY130_assertion; np:hasProvenance dgn-np:NP318066.RApURtsBnWbBT49j8ZFe5jf4If0gUyeSXo_073jetWXxY130_provenance; np:hasPublicationInfo dgn-np:NP318066.RApURtsBnWbBT49j8ZFe5jf4If0gUyeSXo_073jetWXxY130_publicationInfo; a np:Nanopublication . dgn-np:NP318066.RApURtsBnWbBT49j8ZFe5jf4If0gUyeSXo_073jetWXxY130_assertion a np:Assertion . dgn-np:NP318066.RApURtsBnWbBT49j8ZFe5jf4If0gUyeSXo_073jetWXxY130_provenance a np:Provenance . dgn-np:NP318066.RApURtsBnWbBT49j8ZFe5jf4If0gUyeSXo_073jetWXxY130_publicationInfo a np:PublicationInfo . } dgn-np:NP318066.RApURtsBnWbBT49j8ZFe5jf4If0gUyeSXo_073jetWXxY130_assertion { miriam-gene:1243 a ncit:C16612 . lld:C0006826 a ncit:C7057 . dgn-gda:DGN1d3fbcfb0efec9ec61c404959c7f7ef5 sio:SIO_000628 miriam-gene:1243, lld:C0006826; a sio:SIO_001121 . } dgn-np:NP318066.RApURtsBnWbBT49j8ZFe5jf4If0gUyeSXo_073jetWXxY130_provenance { dgn-np:NP318066.RApURtsBnWbBT49j8ZFe5jf4If0gUyeSXo_073jetWXxY130_assertion dcterms:description "[Significant heterogeneity was also found among the families; three of the nine families had marked excess in numbers of systemic cancers, and the remaining families had normal numbers of cancers among the known FAMMM gene carriers and their first degree relatives.]. 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:2372499; 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:NP318066.RApURtsBnWbBT49j8ZFe5jf4If0gUyeSXo_073jetWXxY130_publicationInfo { this: dcterms:created "2015-08-25T14:40:43+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" . }