@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:NP1342633.RAOjMNKK4j0TB4Z81ufsi9viknHpFwU8kPRFM3pYuVcZE130_head { this: np:hasAssertion dgn-np:NP1342633.RAOjMNKK4j0TB4Z81ufsi9viknHpFwU8kPRFM3pYuVcZE130_assertion; np:hasProvenance dgn-np:NP1342633.RAOjMNKK4j0TB4Z81ufsi9viknHpFwU8kPRFM3pYuVcZE130_provenance; np:hasPublicationInfo dgn-np:NP1342633.RAOjMNKK4j0TB4Z81ufsi9viknHpFwU8kPRFM3pYuVcZE130_publicationInfo; a np:Nanopublication . dgn-np:NP1342633.RAOjMNKK4j0TB4Z81ufsi9viknHpFwU8kPRFM3pYuVcZE130_assertion a np:Assertion . dgn-np:NP1342633.RAOjMNKK4j0TB4Z81ufsi9viknHpFwU8kPRFM3pYuVcZE130_provenance a np:Provenance . dgn-np:NP1342633.RAOjMNKK4j0TB4Z81ufsi9viknHpFwU8kPRFM3pYuVcZE130_publicationInfo a np:PublicationInfo . } dgn-np:NP1342633.RAOjMNKK4j0TB4Z81ufsi9viknHpFwU8kPRFM3pYuVcZE130_assertion { miriam-gene:1756 a ncit:C16612 . lld:C0026850 a ncit:C7057 . dgn-gda:DGN5bea89786e769e285deea294e5308056 sio:SIO_000628 miriam-gene:1756, lld:C0026850; a sio:SIO_001121 . } dgn-np:NP1342633.RAOjMNKK4j0TB4Z81ufsi9viknHpFwU8kPRFM3pYuVcZE130_provenance { dgn-np:NP1342633.RAOjMNKK4j0TB4Z81ufsi9viknHpFwU8kPRFM3pYuVcZE130_assertion dcterms:description "[The results indicate that immunohistochemical analysis of dystrophin staining is a valuable diagnostic test for DMD carriers when DNA for testing is unavailable from critical family members or is uninformative, when creatine kinase (CK) values are conflicting or when CK values must be used in isolation.]. 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:8467428; 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:NP1342633.RAOjMNKK4j0TB4Z81ufsi9viknHpFwU8kPRFM3pYuVcZE130_publicationInfo { this: dcterms:created "2016-05-13T12:51:55+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" . }