@prefix dct: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP933511.RALVgwxPsz1Q6zoOf902ObX9UzphbdXNqLsRMF2OK98Q4> .
@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 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:NP933511.RALVgwxPsz1Q6zoOf902ObX9UzphbdXNqLsRMF2OK98Q4130_head {
  this: np:hasAssertion dgn-np:NP933511.RALVgwxPsz1Q6zoOf902ObX9UzphbdXNqLsRMF2OK98Q4130_assertion;
    np:hasProvenance dgn-np:NP933511.RALVgwxPsz1Q6zoOf902ObX9UzphbdXNqLsRMF2OK98Q4130_provenance;
    np:hasPublicationInfo dgn-np:NP933511.RALVgwxPsz1Q6zoOf902ObX9UzphbdXNqLsRMF2OK98Q4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP933511.RALVgwxPsz1Q6zoOf902ObX9UzphbdXNqLsRMF2OK98Q4130_assertion a np:Assertion .
  
  dgn-np:NP933511.RALVgwxPsz1Q6zoOf902ObX9UzphbdXNqLsRMF2OK98Q4130_provenance a np:Provenance .
  
  dgn-np:NP933511.RALVgwxPsz1Q6zoOf902ObX9UzphbdXNqLsRMF2OK98Q4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP933511.RALVgwxPsz1Q6zoOf902ObX9UzphbdXNqLsRMF2OK98Q4130_assertion {
  miriam-gene:7045 a ncit:C16612 .
  
  lld:C0010034 a ncit:C7057 .
  
  dgn-gda:DGNc6acc8866b03a5d80179b7fc081d8ba8 sio:SIO_000628 miriam-gene:7045, lld:C0010034;
    a sio:SIO_001121 .
}

dgn-np:NP933511.RALVgwxPsz1Q6zoOf902ObX9UzphbdXNqLsRMF2OK98Q4130_provenance {
  dgn-np:NP933511.RALVgwxPsz1Q6zoOf902ObX9UzphbdXNqLsRMF2OK98Q4130_assertion dct:description
      "[Several inherited corneal disorders in humans result from mutations in the transforming growth factor beta induced gene (TGFBI), which encodes for the extracellular transforming growth factor beta induced protein (TGFBIp) that is one of the most abundant proteins in the cornea.]. 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:17653042;
    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:NP933511.RALVgwxPsz1Q6zoOf902ObX9UzphbdXNqLsRMF2OK98Q4130_publicationInfo {
  this: dct:created "2014-10-02T12:41:32+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct: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" .
}