@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4> .
@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:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_head {
  this: np:hasAssertion dgn-np:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_assertion;
    np:hasProvenance dgn-np:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_provenance;
    np:hasPublicationInfo dgn-np:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_assertion a np:Assertion .
  
  dgn-np:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_provenance a np:Provenance .
  
  dgn-np:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_assertion {
  miriam-gene:60675 a ncit:C16612 .
  
  lld:C0162809 a ncit:C7057 .
  
  dgn-gda:DGN183eafa83b8f681e641c5b9d2cfbb854 sio:SIO_000628 miriam-gene:60675, lld:C0162809;
    a sio:SIO_001121 .
}

dgn-np:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_provenance {
  dgn-np:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_assertion dcterms:description
      "[Some cases of mutations of FGFR1, and more rarely of its ligand FGF8, or of PROKR2 or its ligand PROK2 have been shown in women suffering from Kallmann syndrome or its hyposmic or normosmic variant.]. 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:20363464;
    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:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:49+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" .
}