@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1282907.RAW3B-bis_VBamcs2GQDukr3bD7Vb8tOCNlOcj6YL00Xw> .
@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/v4.0.0/void/> .

dgn-np:NP1282907.RAW3B-bis_VBamcs2GQDukr3bD7Vb8tOCNlOcj6YL00Xw130_head {
  this: np:hasAssertion dgn-np:NP1282907.RAW3B-bis_VBamcs2GQDukr3bD7Vb8tOCNlOcj6YL00Xw130_assertion;
    np:hasProvenance dgn-np:NP1282907.RAW3B-bis_VBamcs2GQDukr3bD7Vb8tOCNlOcj6YL00Xw130_provenance;
    np:hasPublicationInfo dgn-np:NP1282907.RAW3B-bis_VBamcs2GQDukr3bD7Vb8tOCNlOcj6YL00Xw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1282907.RAW3B-bis_VBamcs2GQDukr3bD7Vb8tOCNlOcj6YL00Xw130_assertion a np:Assertion .
  
  dgn-np:NP1282907.RAW3B-bis_VBamcs2GQDukr3bD7Vb8tOCNlOcj6YL00Xw130_provenance a np:Provenance .
  
  dgn-np:NP1282907.RAW3B-bis_VBamcs2GQDukr3bD7Vb8tOCNlOcj6YL00Xw130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1282907.RAW3B-bis_VBamcs2GQDukr3bD7Vb8tOCNlOcj6YL00Xw130_assertion {
  miriam-gene:57674 a ncit:C16612 .
  
  lld:C0038449 a ncit:C7057 .
  
  dgn-gda:DGNc0574b2a13f849b66ec3497040c2e028 sio:SIO_000628 miriam-gene:57674, lld:C0038449;
    a sio:SIO_001121 .
}

dgn-np:NP1282907.RAW3B-bis_VBamcs2GQDukr3bD7Vb8tOCNlOcj6YL00Xw130_provenance {
  dgn-np:NP1282907.RAW3B-bis_VBamcs2GQDukr3bD7Vb8tOCNlOcj6YL00Xw130_assertion dcterms:description
      "[Since 30.6% (11/36) of Taiwanese moyamoya patients carry an RNF213 mutation and intracranial arterial stenosis was found in half of the asymptomatic mutant carriers, it is suggested that the RNF213 mutation should form part of the diagnostic workup for MMD in clinical practice.]. 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:25956231;
    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:NP1282907.RAW3B-bis_VBamcs2GQDukr3bD7Vb8tOCNlOcj6YL00Xw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:27+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}