@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP290428.RAN447Hr2sCXWXWb6AIyK0yxQ4I-HbTYzP8rBEH63SPXQ> .
@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:NP290428.RAN447Hr2sCXWXWb6AIyK0yxQ4I-HbTYzP8rBEH63SPXQ130_head {
  this: np:hasAssertion dgn-np:NP290428.RAN447Hr2sCXWXWb6AIyK0yxQ4I-HbTYzP8rBEH63SPXQ130_assertion;
    np:hasProvenance dgn-np:NP290428.RAN447Hr2sCXWXWb6AIyK0yxQ4I-HbTYzP8rBEH63SPXQ130_provenance;
    np:hasPublicationInfo dgn-np:NP290428.RAN447Hr2sCXWXWb6AIyK0yxQ4I-HbTYzP8rBEH63SPXQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP290428.RAN447Hr2sCXWXWb6AIyK0yxQ4I-HbTYzP8rBEH63SPXQ130_assertion a np:Assertion .
  
  dgn-np:NP290428.RAN447Hr2sCXWXWb6AIyK0yxQ4I-HbTYzP8rBEH63SPXQ130_provenance a np:Provenance .
  
  dgn-np:NP290428.RAN447Hr2sCXWXWb6AIyK0yxQ4I-HbTYzP8rBEH63SPXQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP290428.RAN447Hr2sCXWXWb6AIyK0yxQ4I-HbTYzP8rBEH63SPXQ130_assertion {
  miriam-gene:4313 a ncit:C16612 .
  
  lld:C0003864 a ncit:C7057 .
  
  dgn-gda:DGN6a0e177939b1aed6c744f5c03fa23979 sio:SIO_000628 miriam-gene:4313, lld:C0003864;
    a sio:SIO_001121 .
}

dgn-np:NP290428.RAN447Hr2sCXWXWb6AIyK0yxQ4I-HbTYzP8rBEH63SPXQ130_provenance {
  dgn-np:NP290428.RAN447Hr2sCXWXWb6AIyK0yxQ4I-HbTYzP8rBEH63SPXQ130_assertion dcterms:description
      "[The discovery that deficiency of this well-characterized gelatinase/collagenase results in an inherited form of an osteolytic and arthritic disorder provides an invaluable insights for the understanding of osteolysis and arthritis and is the first genetic evidence that MMP2 deficiency is important in growth and development.]. 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:15756348;
    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:NP290428.RAN447Hr2sCXWXWb6AIyK0yxQ4I-HbTYzP8rBEH63SPXQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:45+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" .
}