@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI> .
@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:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_head {
  this: np:hasAssertion dgn-np:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_assertion;
    np:hasProvenance dgn-np:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_provenance;
    np:hasPublicationInfo dgn-np:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_assertion a np:Assertion .
  
  dgn-np:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_provenance a np:Provenance .
  
  dgn-np:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_assertion {
  miriam-gene:960 a ncit:C16612 .
  
  lld:C0233643 a ncit:C7057 .
  
  dgn-gda:DGN48a5a141f573ca4ac8ab402401712b40 sio:SIO_000628 miriam-gene:960, lld:C0233643;
    a sio:SIO_001121 .
}

dgn-np:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_provenance {
  dgn-np:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_assertion dcterms:description
      "[This fact and the huge potential number of different CD44 splice variants that can contain v3 and v6 domains can explain incoherence of clinical studies regarding functional asessment of CD44 variants, as well as diminish the chances of using CD44 variants for predictive purpose.]. 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:23151220;
    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:NP296075.RApapQLuFayvwnVxJZXHC_rfbsTk6E3Bm-fcYeWNVpaYI130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:29+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" .
}