@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y> .
@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:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_head {
  this: np:hasAssertion dgn-np:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_assertion;
    np:hasProvenance dgn-np:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_provenance;
    np:hasPublicationInfo dgn-np:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_assertion a np:Assertion .
  
  dgn-np:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_provenance a np:Provenance .
  
  dgn-np:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_assertion {
  miriam-gene:2335 a ncit:C16612 .
  
  lld:C0410179 a ncit:C7057 .
  
  dgn-gda:DGNbfffe5af09e4d9528a100ac8afba22d4 sio:SIO_000628 miriam-gene:2335, lld:C0410179;
    a sio:SIO_001121 .
}

dgn-np:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_provenance {
  dgn-np:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_assertion dcterms:description
      "[These results suggest that collagen VI deficiency may lead to the reduction of fibronectin receptors and that an abnormality of cell adhesion may be involved in the pathogenesis of Ullrich's disease.]. 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:12402292;
    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:NP318159.RAZsrTjywMNWVoytfJHseiV4MpPcfcaJNhXX8XlHag-_Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:04+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" .
}