@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:NP291707.RAUDFh1RDvg7lHO8XG9squ3QHHVpKMbVE1aOxxGW24bTo130_head { this: np:hasAssertion dgn-np:NP291707.RAUDFh1RDvg7lHO8XG9squ3QHHVpKMbVE1aOxxGW24bTo130_assertion; np:hasProvenance dgn-np:NP291707.RAUDFh1RDvg7lHO8XG9squ3QHHVpKMbVE1aOxxGW24bTo130_provenance; np:hasPublicationInfo dgn-np:NP291707.RAUDFh1RDvg7lHO8XG9squ3QHHVpKMbVE1aOxxGW24bTo130_publicationInfo; a np:Nanopublication . dgn-np:NP291707.RAUDFh1RDvg7lHO8XG9squ3QHHVpKMbVE1aOxxGW24bTo130_assertion a np:Assertion . dgn-np:NP291707.RAUDFh1RDvg7lHO8XG9squ3QHHVpKMbVE1aOxxGW24bTo130_provenance a np:Provenance . dgn-np:NP291707.RAUDFh1RDvg7lHO8XG9squ3QHHVpKMbVE1aOxxGW24bTo130_publicationInfo a np:PublicationInfo . } dgn-np:NP291707.RAUDFh1RDvg7lHO8XG9squ3QHHVpKMbVE1aOxxGW24bTo130_assertion { miriam-gene:1756 a ncit:C16612 . lld:C0026850 a ncit:C7057 . dgn-gda:DGN5b56cbee06e297c586951d8f0154d4ed sio:SIO_000628 miriam-gene:1756, lld:C0026850; a sio:SIO_001121 . } dgn-np:NP291707.RAUDFh1RDvg7lHO8XG9squ3QHHVpKMbVE1aOxxGW24bTo130_provenance { dgn-np:NP291707.RAUDFh1RDvg7lHO8XG9squ3QHHVpKMbVE1aOxxGW24bTo130_assertion dcterms:description "[The discovery of the dystrophin gene, whose mutations lead to Duchenne's and Becker's muscular dystrophy (DMD and BMD), represents the first important landmark by which, in the last ten years, molecular biology and genetic studies have revealed many of the molecular defects of the major muscular dystrophies.]. 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:10937856; 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:NP291707.RAUDFh1RDvg7lHO8XG9squ3QHHVpKMbVE1aOxxGW24bTo130_publicationInfo { this: dcterms:created "2016-05-13T12:43:58+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" . }