@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP77316.RALA2Jk9wpvA3a4Pmcw5fEszirbUksn_BmQobJfTSpBAs> .
@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:NP77316.RALA2Jk9wpvA3a4Pmcw5fEszirbUksn_BmQobJfTSpBAs130_head {
  this: np:hasAssertion dgn-np:NP77316.RALA2Jk9wpvA3a4Pmcw5fEszirbUksn_BmQobJfTSpBAs130_assertion;
    np:hasProvenance dgn-np:NP77316.RALA2Jk9wpvA3a4Pmcw5fEszirbUksn_BmQobJfTSpBAs130_provenance;
    np:hasPublicationInfo dgn-np:NP77316.RALA2Jk9wpvA3a4Pmcw5fEszirbUksn_BmQobJfTSpBAs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP77316.RALA2Jk9wpvA3a4Pmcw5fEszirbUksn_BmQobJfTSpBAs130_assertion a np:Assertion .
  
  dgn-np:NP77316.RALA2Jk9wpvA3a4Pmcw5fEszirbUksn_BmQobJfTSpBAs130_provenance a np:Provenance .
  
  dgn-np:NP77316.RALA2Jk9wpvA3a4Pmcw5fEszirbUksn_BmQobJfTSpBAs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP77316.RALA2Jk9wpvA3a4Pmcw5fEszirbUksn_BmQobJfTSpBAs130_assertion {
  miriam-gene:1285 a ncit:C16612 .
  
  lld:C0022578 a ncit:C7057 .
  
  dgn-gda:DGNeaf02e40fecd321a44119c6d2a6ca77d sio:SIO_000628 miriam-gene:1285, lld:C0022578;
    a sio:SIO_001122 .
}

dgn-np:NP77316.RALA2Jk9wpvA3a4Pmcw5fEszirbUksn_BmQobJfTSpBAs130_provenance {
  dgn-np:NP77316.RALA2Jk9wpvA3a4Pmcw5fEszirbUksn_BmQobJfTSpBAs130_assertion dcterms:description
      "[Analysis of COL4A3 and COL4A4 revealed no mutations related to KC patients, but specific genotypes of seven previously described polymorphisms are significantly associated with KC under dominant, recessive, or additive models.]. 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:20029656;
    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:NP77316.RALA2Jk9wpvA3a4Pmcw5fEszirbUksn_BmQobJfTSpBAs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:37+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" .
}