@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:NP655032.RAbeyoEjQKZrrsC5Pp2p8Xej7lsX6q4Z8_QkM8XnJJgHA130_head { this: np:hasAssertion dgn-np:NP655032.RAbeyoEjQKZrrsC5Pp2p8Xej7lsX6q4Z8_QkM8XnJJgHA130_assertion; np:hasProvenance dgn-np:NP655032.RAbeyoEjQKZrrsC5Pp2p8Xej7lsX6q4Z8_QkM8XnJJgHA130_provenance; np:hasPublicationInfo dgn-np:NP655032.RAbeyoEjQKZrrsC5Pp2p8Xej7lsX6q4Z8_QkM8XnJJgHA130_publicationInfo; a np:Nanopublication . dgn-np:NP655032.RAbeyoEjQKZrrsC5Pp2p8Xej7lsX6q4Z8_QkM8XnJJgHA130_assertion a np:Assertion . dgn-np:NP655032.RAbeyoEjQKZrrsC5Pp2p8Xej7lsX6q4Z8_QkM8XnJJgHA130_provenance a np:Provenance . dgn-np:NP655032.RAbeyoEjQKZrrsC5Pp2p8Xej7lsX6q4Z8_QkM8XnJJgHA130_publicationInfo a np:PublicationInfo . } dgn-np:NP655032.RAbeyoEjQKZrrsC5Pp2p8Xej7lsX6q4Z8_QkM8XnJJgHA130_assertion { miriam-gene:1756 a ncit:C16612 . lld:C3542021 a ncit:C7057 . dgn-gda:DGN19b152dbfa43dd8b5201056d69c1418e sio:SIO_000628 miriam-gene:1756, lld:C3542021; a sio:SIO_001121 . } dgn-np:NP655032.RAbeyoEjQKZrrsC5Pp2p8Xej7lsX6q4Z8_QkM8XnJJgHA130_provenance { dgn-np:NP655032.RAbeyoEjQKZrrsC5Pp2p8Xej7lsX6q4Z8_QkM8XnJJgHA130_assertion dcterms:description "[Since the identification of dystrophin as the protein product of the Duchenne and Becker muscular dystrophy locus, many different mutations, encompassing the entire spectrum of gene mutations ranging from point mutations to large deletions, have been found.]. 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:18268530; 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:NP655032.RAbeyoEjQKZrrsC5Pp2p8Xej7lsX6q4Z8_QkM8XnJJgHA130_publicationInfo { this: dcterms:created "2016-05-13T12:46:42+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" . }