@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP878755.RAvXiJdffjGbq3HM-fBfO2IytlOGbgKGVYYkZCwdQnyl4> .
@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:NP878755.RAvXiJdffjGbq3HM-fBfO2IytlOGbgKGVYYkZCwdQnyl4130_head {
  this: np:hasAssertion dgn-np:NP878755.RAvXiJdffjGbq3HM-fBfO2IytlOGbgKGVYYkZCwdQnyl4130_assertion;
    np:hasProvenance dgn-np:NP878755.RAvXiJdffjGbq3HM-fBfO2IytlOGbgKGVYYkZCwdQnyl4130_provenance;
    np:hasPublicationInfo dgn-np:NP878755.RAvXiJdffjGbq3HM-fBfO2IytlOGbgKGVYYkZCwdQnyl4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP878755.RAvXiJdffjGbq3HM-fBfO2IytlOGbgKGVYYkZCwdQnyl4130_assertion a np:Assertion .
  
  dgn-np:NP878755.RAvXiJdffjGbq3HM-fBfO2IytlOGbgKGVYYkZCwdQnyl4130_provenance a np:Provenance .
  
  dgn-np:NP878755.RAvXiJdffjGbq3HM-fBfO2IytlOGbgKGVYYkZCwdQnyl4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP878755.RAvXiJdffjGbq3HM-fBfO2IytlOGbgKGVYYkZCwdQnyl4130_assertion {
  miriam-gene:10205 a ncit:C16612 .
  
  lld:C0019247 a ncit:C7057 .
  
  dgn-gda:DGN781011d7d0dd165564057a359725ca5d sio:SIO_000628 miriam-gene:10205, lld:C0019247;
    a sio:SIO_001121 .
}

dgn-np:NP878755.RAvXiJdffjGbq3HM-fBfO2IytlOGbgKGVYYkZCwdQnyl4130_provenance {
  dgn-np:NP878755.RAvXiJdffjGbq3HM-fBfO2IytlOGbgKGVYYkZCwdQnyl4130_assertion dcterms:description
      "[Results of the rc mouse study, 3D structure predictions, homology with Myelin Protein Zero and EVA1, comprehensive database analyses of polymorphisms and mutations within the human MPZL3 gene and its cell, tissue expression and immunostaining pattern indicate that homozygous or compound heterozygous mutations of MPZL3 might be involved in immune-mediated human hereditary disorders with hair loss.]. 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:19054061;
    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:NP878755.RAvXiJdffjGbq3HM-fBfO2IytlOGbgKGVYYkZCwdQnyl4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:57+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" .
}