@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA> .
@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:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_head {
  this: np:hasAssertion dgn-np:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_assertion;
    np:hasProvenance dgn-np:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_provenance;
    np:hasPublicationInfo dgn-np:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_assertion a np:Assertion .
  
  dgn-np:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_provenance a np:Provenance .
  
  dgn-np:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_assertion {
  miriam-gene:2335 a ncit:C16612 .
  
  lld:C0410179 a ncit:C7057 .
  
  dgn-gda:DGN74cfbf6314176040d095e8bf672bbf26 sio:SIO_000628 miriam-gene:2335, lld:C0410179;
    a sio:SIO_001121 .
}

dgn-np:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_provenance {
  dgn-np:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_assertion dcterms:description
      "[Recently we found a marked reduction of fibronectin receptors in the skin and cultured fibroblasts of two patients with Ullrich's disease with collagen VI deficiency, and speculated that an abnormality of cell adhesion may be involved in the pathogenesis of the 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:16258947;
    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:NP313399.RAzynR7hnXxqMRcPNExkj5sQTWxQDWaolcO2gy1PAiwqA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:59+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" .
}