@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc> .
@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:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_head {
  this: np:hasAssertion dgn-np:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_assertion;
    np:hasProvenance dgn-np:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_provenance;
    np:hasPublicationInfo dgn-np:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_assertion a np:Assertion .
  
  dgn-np:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_provenance a np:Provenance .
  
  dgn-np:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_assertion {
  miriam-gene:3730 a ncit:C16612 .
  
  lld:C0162809 a ncit:C7057 .
  
  dgn-gda:DGN40faaff324772b21081370ad15bdab4a sio:SIO_000628 miriam-gene:3730, lld:C0162809;
    a sio:SIO_001121 .
}

dgn-np:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_provenance {
  dgn-np:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_assertion dcterms:description
      "[Sequence variations may be pseudogene products rather than true polymorphisms, so we should always determine if the position where the variation is located differs between KAL1 and its pseudogene, because it has been suggested that the presence of various polymorphisms in affected individuals could be the cause of KS.]. 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:15636431;
    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:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:20+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" .
}