@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP594407.RA-DzEEkKfp0gMTr_JUXAV3lUHlPQi0l80kDSHyBNHTwg> .
@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/v4.0.0/void/> .

dgn-np:NP594407.RA-DzEEkKfp0gMTr_JUXAV3lUHlPQi0l80kDSHyBNHTwg130_head {
  this: np:hasAssertion dgn-np:NP594407.RA-DzEEkKfp0gMTr_JUXAV3lUHlPQi0l80kDSHyBNHTwg130_assertion;
    np:hasProvenance dgn-np:NP594407.RA-DzEEkKfp0gMTr_JUXAV3lUHlPQi0l80kDSHyBNHTwg130_provenance;
    np:hasPublicationInfo dgn-np:NP594407.RA-DzEEkKfp0gMTr_JUXAV3lUHlPQi0l80kDSHyBNHTwg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP594407.RA-DzEEkKfp0gMTr_JUXAV3lUHlPQi0l80kDSHyBNHTwg130_assertion a np:Assertion .
  
  dgn-np:NP594407.RA-DzEEkKfp0gMTr_JUXAV3lUHlPQi0l80kDSHyBNHTwg130_provenance a np:Provenance .
  
  dgn-np:NP594407.RA-DzEEkKfp0gMTr_JUXAV3lUHlPQi0l80kDSHyBNHTwg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP594407.RA-DzEEkKfp0gMTr_JUXAV3lUHlPQi0l80kDSHyBNHTwg130_assertion {
  miriam-gene:1311 a ncit:C16612 .
  
  lld:C0007302 a ncit:C7057 .
  
  dgn-gda:DGN2b94fd35144b372de1d251cbe03c64db sio:SIO_000628 miriam-gene:1311, lld:C0007302;
    a sio:SIO_001121 .
}

dgn-np:NP594407.RA-DzEEkKfp0gMTr_JUXAV3lUHlPQi0l80kDSHyBNHTwg130_provenance {
  dgn-np:NP594407.RA-DzEEkKfp0gMTr_JUXAV3lUHlPQi0l80kDSHyBNHTwg130_assertion dcterms:description
      "[Studies in chondrocytes and cartilage biopsies suggest that the cartilage disease is caused by retention of mutant COMP in the endoplasmic reticulum of chondrocytes and by disruption of the collagen network of the extracellular matrix.]. 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:17307347;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP594407.RA-DzEEkKfp0gMTr_JUXAV3lUHlPQi0l80kDSHyBNHTwg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:15+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}