@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:NP607178.RAJRBsjbRpLkvfXPIFgJ_evSuegTf9jM2XbI7wkVpwtkU130_head { this: np:hasAssertion dgn-np:NP607178.RAJRBsjbRpLkvfXPIFgJ_evSuegTf9jM2XbI7wkVpwtkU130_assertion; np:hasProvenance dgn-np:NP607178.RAJRBsjbRpLkvfXPIFgJ_evSuegTf9jM2XbI7wkVpwtkU130_provenance; np:hasPublicationInfo dgn-np:NP607178.RAJRBsjbRpLkvfXPIFgJ_evSuegTf9jM2XbI7wkVpwtkU130_publicationInfo; a np:Nanopublication . dgn-np:NP607178.RAJRBsjbRpLkvfXPIFgJ_evSuegTf9jM2XbI7wkVpwtkU130_assertion a np:Assertion . dgn-np:NP607178.RAJRBsjbRpLkvfXPIFgJ_evSuegTf9jM2XbI7wkVpwtkU130_provenance a np:Provenance . dgn-np:NP607178.RAJRBsjbRpLkvfXPIFgJ_evSuegTf9jM2XbI7wkVpwtkU130_publicationInfo a np:PublicationInfo . } dgn-np:NP607178.RAJRBsjbRpLkvfXPIFgJ_evSuegTf9jM2XbI7wkVpwtkU130_assertion { miriam-gene:4000 a ncit:C16612 . lld:C0271694 a ncit:C7057 . dgn-gda:DGNc793cbe1ab2c58117ef4f8afc8b47f7e sio:SIO_000628 miriam-gene:4000, lld:C0271694; a sio:SIO_001121 . } dgn-np:NP607178.RAJRBsjbRpLkvfXPIFgJ_evSuegTf9jM2XbI7wkVpwtkU130_provenance { dgn-np:NP607178.RAJRBsjbRpLkvfXPIFgJ_evSuegTf9jM2XbI7wkVpwtkU130_assertion dcterms:description "[For instance, evaluation of the clinical features of carriers of mutant LMNA in kindreds with familial partial lipodystrophy suggests rational, staged intervention using established pharmaceutical agents to prevent cardiovascular complications not just for patients with lipodystrophy but by extension for patients with the common metabolic syndrome.]. 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:17466974; 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:NP607178.RAJRBsjbRpLkvfXPIFgJ_evSuegTf9jM2XbI7wkVpwtkU130_publicationInfo { this: dcterms:created "2016-05-13T12:46:21+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" . }