@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_head {
  this: np:hasAssertion dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_assertion;
    np:hasProvenance dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_provenance;
    np:hasPublicationInfo dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_assertion a np:Assertion .
  
  dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_provenance a np:Provenance .
  
  dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_assertion {
  miriam-gene:23158 a ncit:C16612 .
  
  lld:C0595905 a ncit:C7057 .
  
  dgn-gda:DGN6ef5760934689d8e852c6972d815594a sio:SIO_000628 miriam-gene:23158, lld:C0595905;
    a sio:SIO_001121 .
}

dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_provenance {
  dgn-np:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_assertion dcterms:description
      "[These findings suggest that the common SNPs in the MDR1 gene have no influence on the expression of its transcript in RCC segments as well as in the normal kidney cortex.]. 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:14685825;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP223445.RAsCVV0PL3C9LBBYKbo4NxUoetk19_ybhalddKF2s1clI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:04+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}