@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:NP1363798.RA73fDmxGM-JuFb1CsHIpYsCKOeDWyGRTMWdxxl-IA9kk130_head { this: np:hasAssertion dgn-np:NP1363798.RA73fDmxGM-JuFb1CsHIpYsCKOeDWyGRTMWdxxl-IA9kk130_assertion; np:hasProvenance dgn-np:NP1363798.RA73fDmxGM-JuFb1CsHIpYsCKOeDWyGRTMWdxxl-IA9kk130_provenance; np:hasPublicationInfo dgn-np:NP1363798.RA73fDmxGM-JuFb1CsHIpYsCKOeDWyGRTMWdxxl-IA9kk130_publicationInfo; a np:Nanopublication . dgn-np:NP1363798.RA73fDmxGM-JuFb1CsHIpYsCKOeDWyGRTMWdxxl-IA9kk130_assertion a np:Assertion . dgn-np:NP1363798.RA73fDmxGM-JuFb1CsHIpYsCKOeDWyGRTMWdxxl-IA9kk130_provenance a np:Provenance . dgn-np:NP1363798.RA73fDmxGM-JuFb1CsHIpYsCKOeDWyGRTMWdxxl-IA9kk130_publicationInfo a np:PublicationInfo . } dgn-np:NP1363798.RA73fDmxGM-JuFb1CsHIpYsCKOeDWyGRTMWdxxl-IA9kk130_assertion { miriam-gene:54997 a ncit:C16612 . lld:C0041341 a ncit:C7057 . dgn-gda:DGN0228a9895ca05a26256112a776d2bbb3 sio:SIO_000628 miriam-gene:54997, lld:C0041341; a sio:SIO_001121 . } dgn-np:NP1363798.RA73fDmxGM-JuFb1CsHIpYsCKOeDWyGRTMWdxxl-IA9kk130_provenance { dgn-np:NP1363798.RA73fDmxGM-JuFb1CsHIpYsCKOeDWyGRTMWdxxl-IA9kk130_assertion dcterms:description "[These data support the hypothesis that both the TSC genes act as tumour suppressors and that the manifestations of TSC in patients with germline TSC mutations rise from second hit somatic mutations inactivating the remaining normal copy of the TSC gene.]. 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:8950679; 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:NP1363798.RA73fDmxGM-JuFb1CsHIpYsCKOeDWyGRTMWdxxl-IA9kk130_publicationInfo { this: dcterms:created "2016-05-13T12:52:04+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" . }