@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA> .
@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:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_head {
  this: np:hasAssertion dgn-np:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_assertion;
    np:hasProvenance dgn-np:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_provenance;
    np:hasPublicationInfo dgn-np:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_assertion a np:Assertion .
  
  dgn-np:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_provenance a np:Provenance .
  
  dgn-np:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_assertion {
  miriam-gene:2328 a ncit:C16612 .
  
  lld:C0025517 a ncit:C7057 .
  
  dgn-gda:DGNffe3f418d0c103e75328baebb12750c2 sio:SIO_000628 miriam-gene:2328, lld:C0025517;
    a sio:SIO_001121 .
}

dgn-np:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_provenance {
  dgn-np:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_assertion dcterms:description
      "[Numerous non-synonymous mutations in FMO3 have been identified in patients suffering from this metabolic disorder (e.g., N61S, M66I, P153L, and R492W), but the molecular mechanism(s) underlying the functional deficit attributed to these alleles has not been elucidated.]. 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:17531949;
    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:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:16+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" .
}