@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:NP868164.RAFaEzh55w_LSatezKe8D0Kei4ZgLBuhe6Slc11n0gnhA130_head { this: np:hasAssertion dgn-np:NP868164.RAFaEzh55w_LSatezKe8D0Kei4ZgLBuhe6Slc11n0gnhA130_assertion; np:hasProvenance dgn-np:NP868164.RAFaEzh55w_LSatezKe8D0Kei4ZgLBuhe6Slc11n0gnhA130_provenance; np:hasPublicationInfo dgn-np:NP868164.RAFaEzh55w_LSatezKe8D0Kei4ZgLBuhe6Slc11n0gnhA130_publicationInfo; a np:Nanopublication . dgn-np:NP868164.RAFaEzh55w_LSatezKe8D0Kei4ZgLBuhe6Slc11n0gnhA130_assertion a np:Assertion . dgn-np:NP868164.RAFaEzh55w_LSatezKe8D0Kei4ZgLBuhe6Slc11n0gnhA130_provenance a np:Provenance . dgn-np:NP868164.RAFaEzh55w_LSatezKe8D0Kei4ZgLBuhe6Slc11n0gnhA130_publicationInfo a np:PublicationInfo . } dgn-np:NP868164.RAFaEzh55w_LSatezKe8D0Kei4ZgLBuhe6Slc11n0gnhA130_assertion { miriam-gene:23095 a ncit:C16612 . lld:C0442874 a ncit:C7057 . dgn-gda:DGNe547ce4a2b34b9cddb31e5215990abf7 sio:SIO_000628 miriam-gene:23095, lld:C0442874; a sio:SIO_001121 . } dgn-np:NP868164.RAFaEzh55w_LSatezKe8D0Kei4ZgLBuhe6Slc11n0gnhA130_provenance { dgn-np:NP868164.RAFaEzh55w_LSatezKe8D0Kei4ZgLBuhe6Slc11n0gnhA130_assertion dcterms:description "[This review examines the growing number of identified dHMN genes, discusses recent insights into the functions of these genes and possible pathogenic mechanisms, and looks at the increasing overlap between dHMN and the other neuropathies CMT2 and SMA.]. 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:21902652; 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:NP868164.RAFaEzh55w_LSatezKe8D0Kei4ZgLBuhe6Slc11n0gnhA130_publicationInfo { this: dcterms:created "2015-08-25T14:46:28+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" . }