@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:NP412922.RAmbd29rdlycLtK0LxgcQdZJPyOYFqEFLf5lpVJDUGF0s130_head { this: np:hasAssertion dgn-np:NP412922.RAmbd29rdlycLtK0LxgcQdZJPyOYFqEFLf5lpVJDUGF0s130_assertion; np:hasProvenance dgn-np:NP412922.RAmbd29rdlycLtK0LxgcQdZJPyOYFqEFLf5lpVJDUGF0s130_provenance; np:hasPublicationInfo dgn-np:NP412922.RAmbd29rdlycLtK0LxgcQdZJPyOYFqEFLf5lpVJDUGF0s130_publicationInfo; a np:Nanopublication . dgn-np:NP412922.RAmbd29rdlycLtK0LxgcQdZJPyOYFqEFLf5lpVJDUGF0s130_assertion a np:Assertion . dgn-np:NP412922.RAmbd29rdlycLtK0LxgcQdZJPyOYFqEFLf5lpVJDUGF0s130_provenance a np:Provenance . dgn-np:NP412922.RAmbd29rdlycLtK0LxgcQdZJPyOYFqEFLf5lpVJDUGF0s130_publicationInfo a np:PublicationInfo . } dgn-np:NP412922.RAmbd29rdlycLtK0LxgcQdZJPyOYFqEFLf5lpVJDUGF0s130_assertion { miriam-gene:1756 a ncit:C16612 . lld:C0026850 a ncit:C7057 . dgn-gda:DGNbb21ec975477a97529c2e0b4529b4166 sio:SIO_000628 miriam-gene:1756, lld:C0026850; a sio:SIO_001121 . } dgn-np:NP412922.RAmbd29rdlycLtK0LxgcQdZJPyOYFqEFLf5lpVJDUGF0s130_provenance { dgn-np:NP412922.RAmbd29rdlycLtK0LxgcQdZJPyOYFqEFLf5lpVJDUGF0s130_assertion dcterms:description "[Characterization of the human chromosome-6-related analogue of dystrophin led to the discovery that in Duchenne muscular dystrophy (DMD) this molecule is expressed diffusely at the muscle cell surface and could, in part, compensate for the dystrophin deficiency of DMD.]. 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:1392135; 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:NP412922.RAmbd29rdlycLtK0LxgcQdZJPyOYFqEFLf5lpVJDUGF0s130_publicationInfo { this: dcterms:created "2016-05-13T12:44:52+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" . }