@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP465485.RARfk5VOEzjkOLl2jGGk1vWpwXALRvgizPU9AlT4uveRs> .
@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:NP465485.RARfk5VOEzjkOLl2jGGk1vWpwXALRvgizPU9AlT4uveRs130_head {
   this: np:hasAssertion dgn-np:NP465485.RARfk5VOEzjkOLl2jGGk1vWpwXALRvgizPU9AlT4uveRs130_assertion ;
    np:hasProvenance dgn-np:NP465485.RARfk5VOEzjkOLl2jGGk1vWpwXALRvgizPU9AlT4uveRs130_provenance ;
    np:hasPublicationInfo dgn-np:NP465485.RARfk5VOEzjkOLl2jGGk1vWpwXALRvgizPU9AlT4uveRs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP465485.RARfk5VOEzjkOLl2jGGk1vWpwXALRvgizPU9AlT4uveRs130_assertion a np:Assertion .
  dgn-np:NP465485.RARfk5VOEzjkOLl2jGGk1vWpwXALRvgizPU9AlT4uveRs130_provenance a np:Provenance .
  dgn-np:NP465485.RARfk5VOEzjkOLl2jGGk1vWpwXALRvgizPU9AlT4uveRs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP465485.RARfk5VOEzjkOLl2jGGk1vWpwXALRvgizPU9AlT4uveRs130_assertion {
   miriam-gene:10611 a ncit:C16612 .
  lld:C0002871 a ncit:C7057 .
  dgn-gda:DGN9bb0a28cda111f05c072272f676a8d0a sio:SIO_000628 miriam-gene:10611 , lld:C0002871 ;
    a sio:SIO_001121 .
}
dgn-np:NP465485.RARfk5VOEzjkOLl2jGGk1vWpwXALRvgizPU9AlT4uveRs130_provenance {
   dgn-np:NP465485.RARfk5VOEzjkOLl2jGGk1vWpwXALRvgizPU9AlT4uveRs130_assertion dcterms:description "[In the mouse, Lhx2, which encodes a member of the LIM (Lin-11, Isl-1, and Mec-3) class of homeodomain proteins, was shown to be expressed during early development in the posterior pituitary, eye, and liver, and its expression persists in adulthood in the central nervous system Lhx2(-/-) mice display absence of posterior pituitary and intermediate lobes, malformation of the anterior lobe, anophthalmia, and they die from anemia.]. 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:22535646 ;
    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:NP465485.RARfk5VOEzjkOLl2jGGk1vWpwXALRvgizPU9AlT4uveRs130_publicationInfo {
   this: dcterms:created "2014-10-02T12:36:39+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" .
}