@prefix dc: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP808118.RAJZtJGHpZK1O61178fhSsQwD2w4ZQYHFQVAlY7apwL8I> .
@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:NP808118.RAJZtJGHpZK1O61178fhSsQwD2w4ZQYHFQVAlY7apwL8I130_head {
   this: np:hasAssertion dgn-np:NP808118.RAJZtJGHpZK1O61178fhSsQwD2w4ZQYHFQVAlY7apwL8I130_assertion ;
    np:hasProvenance dgn-np:NP808118.RAJZtJGHpZK1O61178fhSsQwD2w4ZQYHFQVAlY7apwL8I130_provenance ;
    np:hasPublicationInfo dgn-np:NP808118.RAJZtJGHpZK1O61178fhSsQwD2w4ZQYHFQVAlY7apwL8I130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP808118.RAJZtJGHpZK1O61178fhSsQwD2w4ZQYHFQVAlY7apwL8I130_assertion a np:Assertion .
  dgn-np:NP808118.RAJZtJGHpZK1O61178fhSsQwD2w4ZQYHFQVAlY7apwL8I130_provenance a np:Provenance .
  dgn-np:NP808118.RAJZtJGHpZK1O61178fhSsQwD2w4ZQYHFQVAlY7apwL8I130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP808118.RAJZtJGHpZK1O61178fhSsQwD2w4ZQYHFQVAlY7apwL8I130_assertion {
   miriam-gene:10128 a ncit:C16612 .
  lld:C0021359 a ncit:C7057 .
  dgn-gda:DGN4875eec34743440b4b06dd478cba3955 sio:SIO_000628 miriam-gene:10128 , lld:C0021359 ;
    a sio:SIO_001121 .
}
dgn-np:NP808118.RAJZtJGHpZK1O61178fhSsQwD2w4ZQYHFQVAlY7apwL8I130_provenance {
   dgn-np:NP808118.RAJZtJGHpZK1O61178fhSsQwD2w4ZQYHFQVAlY7apwL8I130_assertion dc:description "[In control fertile women, simultaneous intense apical staining of LIFR and gp130 together with faint SOCS1 staining was observed in epithelial cells, whereas the opposite was seen in most women with unexplained infertility.]. 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:18684446 ;
    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:NP808118.RAJZtJGHpZK1O61178fhSsQwD2w4ZQYHFQVAlY7apwL8I130_publicationInfo {
   this: dc:created "2014-10-02T12:40:15+02:00"^^xsd:dateTime ;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dc:rightsHolder dgn-void:IBIGroup ;
    dc:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}