@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP92102.RA6PAUSpCXu9Dof_vLjz29HsbIOm9VjEdmLYyRu_ZCoJk> .
@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:NP92102.RA6PAUSpCXu9Dof_vLjz29HsbIOm9VjEdmLYyRu_ZCoJk130_head {
  this: np:hasAssertion dgn-np:NP92102.RA6PAUSpCXu9Dof_vLjz29HsbIOm9VjEdmLYyRu_ZCoJk130_assertion;
    np:hasProvenance dgn-np:NP92102.RA6PAUSpCXu9Dof_vLjz29HsbIOm9VjEdmLYyRu_ZCoJk130_provenance;
    np:hasPublicationInfo dgn-np:NP92102.RA6PAUSpCXu9Dof_vLjz29HsbIOm9VjEdmLYyRu_ZCoJk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP92102.RA6PAUSpCXu9Dof_vLjz29HsbIOm9VjEdmLYyRu_ZCoJk130_assertion a np:Assertion .
  
  dgn-np:NP92102.RA6PAUSpCXu9Dof_vLjz29HsbIOm9VjEdmLYyRu_ZCoJk130_provenance a np:Provenance .
  
  dgn-np:NP92102.RA6PAUSpCXu9Dof_vLjz29HsbIOm9VjEdmLYyRu_ZCoJk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP92102.RA6PAUSpCXu9Dof_vLjz29HsbIOm9VjEdmLYyRu_ZCoJk130_assertion {
  miriam-gene:6768 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN82ab22661699c7293999bbb091ca4ee4 sio:SIO_000628 miriam-gene:6768, lld:C0006142;
    a sio:SIO_001122 .
}

dgn-np:NP92102.RA6PAUSpCXu9Dof_vLjz29HsbIOm9VjEdmLYyRu_ZCoJk130_provenance {
  dgn-np:NP92102.RA6PAUSpCXu9Dof_vLjz29HsbIOm9VjEdmLYyRu_ZCoJk130_assertion dcterms:description
      "[This is the first study showing that genetic variation in matriptase has clinical importance. The results encourage further study on the genetic variation affecting protein levels and function in type II transmembrane serine proteases.]. 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:20716618;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP92102.RA6PAUSpCXu9Dof_vLjz29HsbIOm9VjEdmLYyRu_ZCoJk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:45+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" .
}