@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP858119.RAakPxA2NIkQ00sIjUbJl3YjL-29UJvx5PS3UA4C4AcSs> .
@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:NP858119.RAakPxA2NIkQ00sIjUbJl3YjL-29UJvx5PS3UA4C4AcSs130_head {
  this: np:hasAssertion dgn-np:NP858119.RAakPxA2NIkQ00sIjUbJl3YjL-29UJvx5PS3UA4C4AcSs130_assertion;
    np:hasProvenance dgn-np:NP858119.RAakPxA2NIkQ00sIjUbJl3YjL-29UJvx5PS3UA4C4AcSs130_provenance;
    np:hasPublicationInfo dgn-np:NP858119.RAakPxA2NIkQ00sIjUbJl3YjL-29UJvx5PS3UA4C4AcSs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP858119.RAakPxA2NIkQ00sIjUbJl3YjL-29UJvx5PS3UA4C4AcSs130_assertion a np:Assertion .
  
  dgn-np:NP858119.RAakPxA2NIkQ00sIjUbJl3YjL-29UJvx5PS3UA4C4AcSs130_provenance a np:Provenance .
  
  dgn-np:NP858119.RAakPxA2NIkQ00sIjUbJl3YjL-29UJvx5PS3UA4C4AcSs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP858119.RAakPxA2NIkQ00sIjUbJl3YjL-29UJvx5PS3UA4C4AcSs130_assertion {
  miriam-gene:3586 a ncit:C16612 .
  
  lld:C0271183 a ncit:C7057 .
  
  dgn-gda:DGNa770f6a82ba41bcbd5014f64b0982ebc sio:SIO_000628 miriam-gene:3586, lld:C0271183;
    a sio:SIO_001121 .
}

dgn-np:NP858119.RAakPxA2NIkQ00sIjUbJl3YjL-29UJvx5PS3UA4C4AcSs130_provenance {
  dgn-np:NP858119.RAakPxA2NIkQ00sIjUbJl3YjL-29UJvx5PS3UA4C4AcSs130_assertion dcterms:description
      "[Four single-nucleotide polymorphisms (SNPs) in the TGIF, lumican, TGFB1, and HGF genes have been declared to be associated with high myopia in Chinese living in southeast China, but none of them has been confirmed by additional studies.]. 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:19060265;
    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:NP858119.RAakPxA2NIkQ00sIjUbJl3YjL-29UJvx5PS3UA4C4AcSs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:44+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" .
}