@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP978884.RA1JHov30j_1dVLee0nFGiByK9rhLVwY2z1RsRd4Vn874> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP978884.RA1JHov30j_1dVLee0nFGiByK9rhLVwY2z1RsRd4Vn874130_head {
  this: np:hasAssertion dgn-np:NP978884.RA1JHov30j_1dVLee0nFGiByK9rhLVwY2z1RsRd4Vn874130_assertion ;
    np:hasProvenance dgn-np:NP978884.RA1JHov30j_1dVLee0nFGiByK9rhLVwY2z1RsRd4Vn874130_provenance ;
    np:hasPublicationInfo dgn-np:NP978884.RA1JHov30j_1dVLee0nFGiByK9rhLVwY2z1RsRd4Vn874130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP978884.RA1JHov30j_1dVLee0nFGiByK9rhLVwY2z1RsRd4Vn874130_assertion a np:Assertion .
  dgn-np:NP978884.RA1JHov30j_1dVLee0nFGiByK9rhLVwY2z1RsRd4Vn874130_provenance a np:Provenance .
  dgn-np:NP978884.RA1JHov30j_1dVLee0nFGiByK9rhLVwY2z1RsRd4Vn874130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP978884.RA1JHov30j_1dVLee0nFGiByK9rhLVwY2z1RsRd4Vn874130_assertion {
  miriam-gene:196527 a ncit:C16612 .
  lld:C0796149 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP978884.RA1JHov30j_1dVLee0nFGiByK9rhLVwY2z1RsRd4Vn874130_provenance {
  dgn-np:NP978884.RA1JHov30j_1dVLee0nFGiByK9rhLVwY2z1RsRd4Vn874130_assertion dcterms:description "[The excitement about Tmem16 proteins has been enhanced by the finding that Ano1 has been linked to cancer, mutations in Ano5 are linked to several forms of muscular dystrophy (LGMDL2 and MMD-3), mutations in Ano10 are linked to autosomal recessive spinocerebellar ataxia, and mutations in Ano6 are linked to Scott syndrome, a rare bleeding disorder.]. 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:21642943 ;
    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:NP978884.RA1JHov30j_1dVLee0nFGiByK9rhLVwY2z1RsRd4Vn874130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:38+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v3.0.0.0" .
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}