@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP763299.RA9ASrBz67I7icF8D_izAIy_iOtfMIMCyir8T6KXzmS6M> .
@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:NP763299.RA9ASrBz67I7icF8D_izAIy_iOtfMIMCyir8T6KXzmS6M130_head {
  this: np:hasAssertion dgn-np:NP763299.RA9ASrBz67I7icF8D_izAIy_iOtfMIMCyir8T6KXzmS6M130_assertion;
    np:hasProvenance dgn-np:NP763299.RA9ASrBz67I7icF8D_izAIy_iOtfMIMCyir8T6KXzmS6M130_provenance;
    np:hasPublicationInfo dgn-np:NP763299.RA9ASrBz67I7icF8D_izAIy_iOtfMIMCyir8T6KXzmS6M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP763299.RA9ASrBz67I7icF8D_izAIy_iOtfMIMCyir8T6KXzmS6M130_assertion a np:Assertion .
  
  dgn-np:NP763299.RA9ASrBz67I7icF8D_izAIy_iOtfMIMCyir8T6KXzmS6M130_provenance a np:Provenance .
  
  dgn-np:NP763299.RA9ASrBz67I7icF8D_izAIy_iOtfMIMCyir8T6KXzmS6M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP763299.RA9ASrBz67I7icF8D_izAIy_iOtfMIMCyir8T6KXzmS6M130_assertion {
  miriam-gene:1282 a ncit:C16612 .
  
  lld:C0265216 a ncit:C7057 .
  
  dgn-gda:DGN67bf5af5c9597595e2772302b1de938d sio:SIO_000628 miriam-gene:1282, lld:C0265216;
    a sio:SIO_001121 .
}

dgn-np:NP763299.RA9ASrBz67I7icF8D_izAIy_iOtfMIMCyir8T6KXzmS6M130_provenance {
  dgn-np:NP763299.RA9ASrBz67I7icF8D_izAIy_iOtfMIMCyir8T6KXzmS6M130_assertion dcterms:description
      "[In this study, we used dermal fibroblasts from eight normal individuals and nine males with XLAS to test the hypotheses that COL4A5 mutations increase transcription of COL4A1 and suppress transcription of COL4A6.]. 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:9749944;
    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:NP763299.RA9ASrBz67I7icF8D_izAIy_iOtfMIMCyir8T6KXzmS6M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:42+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" .
}