@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP373724.RAlDN31UKvYGvBMRgyjLhAQoN6dndCDVMewo_oFw01l0U> .
@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:NP373724.RAlDN31UKvYGvBMRgyjLhAQoN6dndCDVMewo_oFw01l0U130_head {
  this: np:hasAssertion dgn-np:NP373724.RAlDN31UKvYGvBMRgyjLhAQoN6dndCDVMewo_oFw01l0U130_assertion;
    np:hasProvenance dgn-np:NP373724.RAlDN31UKvYGvBMRgyjLhAQoN6dndCDVMewo_oFw01l0U130_provenance;
    np:hasPublicationInfo dgn-np:NP373724.RAlDN31UKvYGvBMRgyjLhAQoN6dndCDVMewo_oFw01l0U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP373724.RAlDN31UKvYGvBMRgyjLhAQoN6dndCDVMewo_oFw01l0U130_assertion a np:Assertion .
  
  dgn-np:NP373724.RAlDN31UKvYGvBMRgyjLhAQoN6dndCDVMewo_oFw01l0U130_provenance a np:Provenance .
  
  dgn-np:NP373724.RAlDN31UKvYGvBMRgyjLhAQoN6dndCDVMewo_oFw01l0U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP373724.RAlDN31UKvYGvBMRgyjLhAQoN6dndCDVMewo_oFw01l0U130_assertion {
  miriam-gene:3973 a ncit:C16612 .
  
  lld:C0342549 a ncit:C7057 .
  
  dgn-gda:DGNe8d59953f0b303f5d770464de5663f0b sio:SIO_000628 miriam-gene:3973, lld:C0342549;
    a sio:SIO_001121 .
}

dgn-np:NP373724.RAlDN31UKvYGvBMRgyjLhAQoN6dndCDVMewo_oFw01l0U130_provenance {
  dgn-np:NP373724.RAlDN31UKvYGvBMRgyjLhAQoN6dndCDVMewo_oFw01l0U130_assertion dcterms:description
      "[Together, these analyses suggest that exon 11 of human LHCGR could be more susceptible to mutation than the other 10 exons together and that activation of LHCGR, contingent to the somatic silencing of neighbouring ALF, could be linked to male-limited precocious puberty and pre-eclampsia.]. 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:16087288;
    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:NP373724.RAlDN31UKvYGvBMRgyjLhAQoN6dndCDVMewo_oFw01l0U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:39+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" .
}