@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:NP933191.RAFUebjKl8Z0tT1-91RdnKnBi3og9O6NWr3zCqlKXjpps130_head { this: np:hasAssertion dgn-np:NP933191.RAFUebjKl8Z0tT1-91RdnKnBi3og9O6NWr3zCqlKXjpps130_assertion; np:hasProvenance dgn-np:NP933191.RAFUebjKl8Z0tT1-91RdnKnBi3og9O6NWr3zCqlKXjpps130_provenance; np:hasPublicationInfo dgn-np:NP933191.RAFUebjKl8Z0tT1-91RdnKnBi3og9O6NWr3zCqlKXjpps130_publicationInfo; a np:Nanopublication . dgn-np:NP933191.RAFUebjKl8Z0tT1-91RdnKnBi3og9O6NWr3zCqlKXjpps130_assertion a np:Assertion . dgn-np:NP933191.RAFUebjKl8Z0tT1-91RdnKnBi3og9O6NWr3zCqlKXjpps130_provenance a np:Provenance . dgn-np:NP933191.RAFUebjKl8Z0tT1-91RdnKnBi3og9O6NWr3zCqlKXjpps130_publicationInfo a np:PublicationInfo . } dgn-np:NP933191.RAFUebjKl8Z0tT1-91RdnKnBi3og9O6NWr3zCqlKXjpps130_assertion { miriam-gene:57760 a ncit:C16612 . lld:C0037773 a ncit:C7057 . dgn-gda:DGN3f852e00ff0fc9bdd4fa4476894e9a38 sio:SIO_000628 miriam-gene:57760, lld:C0037773; a sio:SIO_001121 . } dgn-np:NP933191.RAFUebjKl8Z0tT1-91RdnKnBi3og9O6NWr3zCqlKXjpps130_provenance { dgn-np:NP933191.RAFUebjKl8Z0tT1-91RdnKnBi3og9O6NWr3zCqlKXjpps130_assertion dcterms:description "[Disease worsened in patients with SCA1, SCA2, and SCA3 mutations (mean [SE] increase in CCFSw, +0.014 [0.005] to +0.025 [0.004] per year), improved in patients with SPG4 mutations (mean [SE] increase in CCFSw, -0.012 [0.003] per year; P = .02), and remained stable in patients with SCA6, SCA7, or other SCA mutations (mean [SE] increase in CCFSw, -0.015 [0.011] to +0.009 [0.013] per year) or hereditary spastic paraplegia with other SPG mutations (mean [SE] increase in CCFSw, -0.005 [0.005] per year).]. 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:22491195; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP933191.RAFUebjKl8Z0tT1-91RdnKnBi3og9O6NWr3zCqlKXjpps130_publicationInfo { this: dcterms:created "2015-08-25T14:47:10+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" . }