@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:NP761004.RAq6F15UwaC90NsibiFK-rQRB1Ii_2Gbaxfh7XLgOACI4130_head { this: np:hasAssertion dgn-np:NP761004.RAq6F15UwaC90NsibiFK-rQRB1Ii_2Gbaxfh7XLgOACI4130_assertion; np:hasProvenance dgn-np:NP761004.RAq6F15UwaC90NsibiFK-rQRB1Ii_2Gbaxfh7XLgOACI4130_provenance; np:hasPublicationInfo dgn-np:NP761004.RAq6F15UwaC90NsibiFK-rQRB1Ii_2Gbaxfh7XLgOACI4130_publicationInfo; a np:Nanopublication . dgn-np:NP761004.RAq6F15UwaC90NsibiFK-rQRB1Ii_2Gbaxfh7XLgOACI4130_assertion a np:Assertion . dgn-np:NP761004.RAq6F15UwaC90NsibiFK-rQRB1Ii_2Gbaxfh7XLgOACI4130_provenance a np:Provenance . dgn-np:NP761004.RAq6F15UwaC90NsibiFK-rQRB1Ii_2Gbaxfh7XLgOACI4130_publicationInfo a np:PublicationInfo . } dgn-np:NP761004.RAq6F15UwaC90NsibiFK-rQRB1Ii_2Gbaxfh7XLgOACI4130_assertion { miriam-gene:4000 a ncit:C16612 . lld:C0023787 a ncit:C7057 . dgn-gda:DGNb9f525c5636d3a5f86a181bddfabd806 sio:SIO_000628 miriam-gene:4000, lld:C0023787; a sio:SIO_001121 . } dgn-np:NP761004.RAq6F15UwaC90NsibiFK-rQRB1Ii_2Gbaxfh7XLgOACI4130_provenance { dgn-np:NP761004.RAq6F15UwaC90NsibiFK-rQRB1Ii_2Gbaxfh7XLgOACI4130_assertion dcterms:description "[We conducted an open-label prospective study of patients with acquired forms of lipodystrophy and inherited forms of lipodystrophy secondary to mutations in the AGPAT2, SEIPIN (also known as BSCL2), LMNA and PPARgamma (also known as PPARG) genes.]. 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:19727665; 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:NP761004.RAq6F15UwaC90NsibiFK-rQRB1Ii_2Gbaxfh7XLgOACI4130_publicationInfo { this: dcterms:created "2016-05-13T12:47:30+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" . }