@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:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_head { this: np:hasAssertion dgn-np:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_assertion; np:hasProvenance dgn-np:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_provenance; np:hasPublicationInfo dgn-np:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_publicationInfo; a np:Nanopublication . dgn-np:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_assertion a np:Assertion . dgn-np:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_provenance a np:Provenance . dgn-np:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_publicationInfo a np:PublicationInfo . } dgn-np:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_assertion { miriam-gene:1410 a ncit:C16612 . lld:C0026848 a ncit:C7057 . dgn-gda:DGN801a7dc4c69e5222f949c89078863c65 sio:SIO_000628 miriam-gene:1410, lld:C0026848; a sio:SIO_001121 . } dgn-np:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_provenance { dgn-np:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_assertion dcterms:description "[Multiple effects of HspB5 mutations are analyzed, and data are presented indicating that mutations of this protein are accompanied by development of different congenital diseases, such as cataract and different types of myopathies.]. 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:23379525; 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:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_publicationInfo { this: dcterms:created "2016-05-13T12:49:42+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" . }