@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:NP652299.RANhMAtzG_caMTE1pG9GL3yMYzikt5395lTZspbX7iJyg130_head { this: np:hasAssertion dgn-np:NP652299.RANhMAtzG_caMTE1pG9GL3yMYzikt5395lTZspbX7iJyg130_assertion; np:hasProvenance dgn-np:NP652299.RANhMAtzG_caMTE1pG9GL3yMYzikt5395lTZspbX7iJyg130_provenance; np:hasPublicationInfo dgn-np:NP652299.RANhMAtzG_caMTE1pG9GL3yMYzikt5395lTZspbX7iJyg130_publicationInfo; a np:Nanopublication . dgn-np:NP652299.RANhMAtzG_caMTE1pG9GL3yMYzikt5395lTZspbX7iJyg130_assertion a np:Assertion . dgn-np:NP652299.RANhMAtzG_caMTE1pG9GL3yMYzikt5395lTZspbX7iJyg130_provenance a np:Provenance . dgn-np:NP652299.RANhMAtzG_caMTE1pG9GL3yMYzikt5395lTZspbX7iJyg130_publicationInfo a np:PublicationInfo . } dgn-np:NP652299.RANhMAtzG_caMTE1pG9GL3yMYzikt5395lTZspbX7iJyg130_assertion { miriam-gene:1756 a ncit:C16612 . lld:C0917713 a ncit:C7057 . dgn-gda:DGN48730e4b1645f9a71f4d0f9839c80419 sio:SIO_000628 miriam-gene:1756, lld:C0917713; a sio:SIO_001121 . } dgn-np:NP652299.RANhMAtzG_caMTE1pG9GL3yMYzikt5395lTZspbX7iJyg130_provenance { dgn-np:NP652299.RANhMAtzG_caMTE1pG9GL3yMYzikt5395lTZspbX7iJyg130_assertion dcterms:description "[In order to investigate if the same apparent decrease in dystrophin negative fibers with aging observed in mouse mdx female heterozygotes also occurs in carriers of the DMD and BMD gene, we have studied the muscle of 29 DMD carriers (19 adults and 10 young daughters of obligate carriers, including 3 manifesting carriers) and 5 adult asymptomatic heterozygotes for Becker dystrophy (BMD).]. 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:1822792; 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:NP652299.RANhMAtzG_caMTE1pG9GL3yMYzikt5395lTZspbX7iJyg130_publicationInfo { this: dcterms:created "2016-05-13T12:46:41+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" . }