@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_head {
  this: np:hasAssertion dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_assertion;
    np:hasProvenance dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_provenance;
    np:hasPublicationInfo dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_assertion a np:Assertion .
  
  dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_provenance a np:Provenance .
  
  dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_assertion {
  miriam-gene:3973 a ncit:C16612 .
  
  lld:C0342549 a ncit:C7057 .
  
  dgn-gda:DGNcab56e5505df22733c38e1e456d77000 sio:SIO_000628 miriam-gene:3973, lld:C0342549;
    a sio:SIO_001122 .
}

dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_provenance {
  dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_assertion dcterms:description
      "[To generate a mouse model for the human disease, we have introduced an aspartic acid to glycine mutation in amino acid residue 582 (D582G) of the mouse LHR gene corresponding to the most common D578G mutation found in boys with familial male-limited precocious puberty (FMPP).]. 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:23861372;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:02+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}