@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:NP80261.RARST0wVkgfrulwDKgQgFhb3LhEjkG1dlceSSlmP5OACc130_head { this: np:hasAssertion dgn-np:NP80261.RARST0wVkgfrulwDKgQgFhb3LhEjkG1dlceSSlmP5OACc130_assertion; np:hasProvenance dgn-np:NP80261.RARST0wVkgfrulwDKgQgFhb3LhEjkG1dlceSSlmP5OACc130_provenance; np:hasPublicationInfo dgn-np:NP80261.RARST0wVkgfrulwDKgQgFhb3LhEjkG1dlceSSlmP5OACc130_publicationInfo; a np:Nanopublication . dgn-np:NP80261.RARST0wVkgfrulwDKgQgFhb3LhEjkG1dlceSSlmP5OACc130_assertion a np:Assertion . dgn-np:NP80261.RARST0wVkgfrulwDKgQgFhb3LhEjkG1dlceSSlmP5OACc130_provenance a np:Provenance . dgn-np:NP80261.RARST0wVkgfrulwDKgQgFhb3LhEjkG1dlceSSlmP5OACc130_publicationInfo a np:PublicationInfo . } dgn-np:NP80261.RARST0wVkgfrulwDKgQgFhb3LhEjkG1dlceSSlmP5OACc130_assertion { miriam-gene:6606 a ncit:C16612 . lld:C0002736 a ncit:C7057 . dgn-gda:DGN43c086bcc0505e045beb0100c5179e9a sio:SIO_000628 miriam-gene:6606, lld:C0002736; a sio:SIO_001122 . } dgn-np:NP80261.RARST0wVkgfrulwDKgQgFhb3LhEjkG1dlceSSlmP5OACc130_provenance { dgn-np:NP80261.RARST0wVkgfrulwDKgQgFhb3LhEjkG1dlceSSlmP5OACc130_assertion dcterms:description "[These data indicated that there would be no much difference in disease prevalence of SMA compared with western countries. Since the prevalence of SMA is higher than other autosomal recessive disorders, the carrier detection method using real-time PCR coul]. 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:15608400; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP80261.RARST0wVkgfrulwDKgQgFhb3LhEjkG1dlceSSlmP5OACc130_publicationInfo { this: dcterms:created "2015-08-25T14:38:24+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }