@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:NP152675.RAvtwn5h_-egcvhv4Joc8k4raFPLlN9mRJXuH1xC5uPU0130_head { this: np:hasAssertion dgn-np:NP152675.RAvtwn5h_-egcvhv4Joc8k4raFPLlN9mRJXuH1xC5uPU0130_assertion; np:hasProvenance dgn-np:NP152675.RAvtwn5h_-egcvhv4Joc8k4raFPLlN9mRJXuH1xC5uPU0130_provenance; np:hasPublicationInfo dgn-np:NP152675.RAvtwn5h_-egcvhv4Joc8k4raFPLlN9mRJXuH1xC5uPU0130_publicationInfo; a np:Nanopublication . dgn-np:NP152675.RAvtwn5h_-egcvhv4Joc8k4raFPLlN9mRJXuH1xC5uPU0130_assertion a np:Assertion . dgn-np:NP152675.RAvtwn5h_-egcvhv4Joc8k4raFPLlN9mRJXuH1xC5uPU0130_provenance a np:Provenance . dgn-np:NP152675.RAvtwn5h_-egcvhv4Joc8k4raFPLlN9mRJXuH1xC5uPU0130_publicationInfo a np:PublicationInfo . } dgn-np:NP152675.RAvtwn5h_-egcvhv4Joc8k4raFPLlN9mRJXuH1xC5uPU0130_assertion { miriam-gene:1756 a ncit:C16612 . lld:C0013264 a ncit:C7057 . dgn-gda:DGN4e0eacedce467dd480cda857a8e423ea sio:SIO_000628 miriam-gene:1756, lld:C0013264; a sio:SIO_001122 . } dgn-np:NP152675.RAvtwn5h_-egcvhv4Joc8k4raFPLlN9mRJXuH1xC5uPU0130_provenance { dgn-np:NP152675.RAvtwn5h_-egcvhv4Joc8k4raFPLlN9mRJXuH1xC5uPU0130_assertion dcterms:description "[Here, we report one of the largest study based on the comparison of clinical, cognitive, molecular and expression data in a large cohort of 81 patients affected with Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) bearing mutations predicted to affect either all dystrophin products, including Dp71 or all dystrophin products, except Dp71.]. 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:19602481; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP152675.RAvtwn5h_-egcvhv4Joc8k4raFPLlN9mRJXuH1xC5uPU0130_publicationInfo { this: dcterms:created "2016-05-13T12:42:56+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" . }