@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP664312.RAA0rxJI_UW33YX9XkOZFn5tCETwHvwMqCyzOfhxP4Y3k> .
@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:NP664312.RAA0rxJI_UW33YX9XkOZFn5tCETwHvwMqCyzOfhxP4Y3k130_head {
  this: np:hasAssertion dgn-np:NP664312.RAA0rxJI_UW33YX9XkOZFn5tCETwHvwMqCyzOfhxP4Y3k130_assertion ;
    np:hasProvenance dgn-np:NP664312.RAA0rxJI_UW33YX9XkOZFn5tCETwHvwMqCyzOfhxP4Y3k130_provenance ;
    np:hasPublicationInfo dgn-np:NP664312.RAA0rxJI_UW33YX9XkOZFn5tCETwHvwMqCyzOfhxP4Y3k130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP664312.RAA0rxJI_UW33YX9XkOZFn5tCETwHvwMqCyzOfhxP4Y3k130_assertion a np:Assertion .
  dgn-np:NP664312.RAA0rxJI_UW33YX9XkOZFn5tCETwHvwMqCyzOfhxP4Y3k130_provenance a np:Provenance .
  dgn-np:NP664312.RAA0rxJI_UW33YX9XkOZFn5tCETwHvwMqCyzOfhxP4Y3k130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP664312.RAA0rxJI_UW33YX9XkOZFn5tCETwHvwMqCyzOfhxP4Y3k130_assertion {
  miriam-gene:2492 a ncit:C16612 .
  lld:C0271791 a ncit:C7057 .
  dgn-gda:DGN53d40d89b8276342da53917c7abdd061 sio:SIO_000628 miriam-gene:2492 , lld:C0271791 ;
    a sio:SIO_001121 .
}
dgn-np:NP664312.RAA0rxJI_UW33YX9XkOZFn5tCETwHvwMqCyzOfhxP4Y3k130_provenance {
  dgn-np:NP664312.RAA0rxJI_UW33YX9XkOZFn5tCETwHvwMqCyzOfhxP4Y3k130_assertion dcterms:description "[DESIGN, INTERVENTION, AND PATIENTS: After blood sampling, we sequenced the FSHr from genomic leukocytes DNA from eight patients with sOHSS of the first or second trimester of pregnancy with normal or high hCG levels or with high TSH levels associated with severe hypothyroidism.]. 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:16278261 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
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  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:NP664312.RAA0rxJI_UW33YX9XkOZFn5tCETwHvwMqCyzOfhxP4Y3k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:41+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> ;
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}