@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP548823.RAiX-QMxJ0uzM37GlAhRgalxyGbkuLCgeAiK3p-FpkKMk> .
@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:NP548823.RAiX-QMxJ0uzM37GlAhRgalxyGbkuLCgeAiK3p-FpkKMk130_head {
  this: np:hasAssertion dgn-np:NP548823.RAiX-QMxJ0uzM37GlAhRgalxyGbkuLCgeAiK3p-FpkKMk130_assertion;
    np:hasProvenance dgn-np:NP548823.RAiX-QMxJ0uzM37GlAhRgalxyGbkuLCgeAiK3p-FpkKMk130_provenance;
    np:hasPublicationInfo dgn-np:NP548823.RAiX-QMxJ0uzM37GlAhRgalxyGbkuLCgeAiK3p-FpkKMk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP548823.RAiX-QMxJ0uzM37GlAhRgalxyGbkuLCgeAiK3p-FpkKMk130_assertion a np:Assertion .
  
  dgn-np:NP548823.RAiX-QMxJ0uzM37GlAhRgalxyGbkuLCgeAiK3p-FpkKMk130_provenance a np:Provenance .
  
  dgn-np:NP548823.RAiX-QMxJ0uzM37GlAhRgalxyGbkuLCgeAiK3p-FpkKMk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP548823.RAiX-QMxJ0uzM37GlAhRgalxyGbkuLCgeAiK3p-FpkKMk130_assertion {
  miriam-gene:4166 a ncit:C16612 .
  
  lld:C1636149 a ncit:C7057 .
  
  dgn-gda:DGNec27a578d6ceade2a1268ee433041d3f sio:SIO_000628 miriam-gene:4166, lld:C1636149;
    a sio:SIO_001121 .
}

dgn-np:NP548823.RAiX-QMxJ0uzM37GlAhRgalxyGbkuLCgeAiK3p-FpkKMk130_provenance {
  dgn-np:NP548823.RAiX-QMxJ0uzM37GlAhRgalxyGbkuLCgeAiK3p-FpkKMk130_assertion dcterms:description
      "[Moreover, the observation that some cases of MCD cannot be explained by mutations in the coding region of CHST6 suggests that MCD may result from possible upstream rearrangements in the CHST6 genomic region.]. 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:19223992;
    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:NP548823.RAiX-QMxJ0uzM37GlAhRgalxyGbkuLCgeAiK3p-FpkKMk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:04+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}