@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:NP1369970.RApVlKIeKHxXWq2mEkO3VvTFWHEOWIcocfi83ABJL3aXY130_head { this: np:hasAssertion dgn-np:NP1369970.RApVlKIeKHxXWq2mEkO3VvTFWHEOWIcocfi83ABJL3aXY130_assertion; np:hasProvenance dgn-np:NP1369970.RApVlKIeKHxXWq2mEkO3VvTFWHEOWIcocfi83ABJL3aXY130_provenance; np:hasPublicationInfo dgn-np:NP1369970.RApVlKIeKHxXWq2mEkO3VvTFWHEOWIcocfi83ABJL3aXY130_publicationInfo; a np:Nanopublication . dgn-np:NP1369970.RApVlKIeKHxXWq2mEkO3VvTFWHEOWIcocfi83ABJL3aXY130_assertion a np:Assertion . dgn-np:NP1369970.RApVlKIeKHxXWq2mEkO3VvTFWHEOWIcocfi83ABJL3aXY130_provenance a np:Provenance . dgn-np:NP1369970.RApVlKIeKHxXWq2mEkO3VvTFWHEOWIcocfi83ABJL3aXY130_publicationInfo a np:PublicationInfo . } dgn-np:NP1369970.RApVlKIeKHxXWq2mEkO3VvTFWHEOWIcocfi83ABJL3aXY130_assertion { miriam-gene:7439 a ncit:C16612 . lld:C0917713 a ncit:C7057 . dgn-gda:DGNaaa3e0c3a7fa2a5e88716368f7b68cd7 sio:SIO_000628 miriam-gene:7439, lld:C0917713; a sio:SIO_001121 . } dgn-np:NP1369970.RApVlKIeKHxXWq2mEkO3VvTFWHEOWIcocfi83ABJL3aXY130_provenance { dgn-np:NP1369970.RApVlKIeKHxXWq2mEkO3VvTFWHEOWIcocfi83ABJL3aXY130_assertion dcterms:description "[Using the polymerase chain reaction method (PCR), we examined the allele frequencies and heterozygosities of 7 polymorphic sites (pERT87, and CA polymorphisms in the 5' and 3' regions) of the dystrophin gene in 20 Japanese Duchenne muscular dystrophy and Becker muscular dystrophy (DMD or BMD) families consisting of 36 males, including 23 cases of DMD and BMD, and 28 females.]. 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:9088109; 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:NP1369970.RApVlKIeKHxXWq2mEkO3VvTFWHEOWIcocfi83ABJL3aXY130_publicationInfo { this: dcterms:created "2016-05-13T12:52:07+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" . }