@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP233195.RA83m36ujC0ZgE3K_XkqcGQ74gC_flcTRaVXbII02-5i8> .
@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:NP233195.RA83m36ujC0ZgE3K_XkqcGQ74gC_flcTRaVXbII02-5i8130_head {
  this: np:hasAssertion dgn-np:NP233195.RA83m36ujC0ZgE3K_XkqcGQ74gC_flcTRaVXbII02-5i8130_assertion;
    np:hasProvenance dgn-np:NP233195.RA83m36ujC0ZgE3K_XkqcGQ74gC_flcTRaVXbII02-5i8130_provenance;
    np:hasPublicationInfo dgn-np:NP233195.RA83m36ujC0ZgE3K_XkqcGQ74gC_flcTRaVXbII02-5i8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP233195.RA83m36ujC0ZgE3K_XkqcGQ74gC_flcTRaVXbII02-5i8130_assertion a np:Assertion .
  
  dgn-np:NP233195.RA83m36ujC0ZgE3K_XkqcGQ74gC_flcTRaVXbII02-5i8130_provenance a np:Provenance .
  
  dgn-np:NP233195.RA83m36ujC0ZgE3K_XkqcGQ74gC_flcTRaVXbII02-5i8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP233195.RA83m36ujC0ZgE3K_XkqcGQ74gC_flcTRaVXbII02-5i8130_assertion {
  miriam-gene:10518 a ncit:C16612 .
  
  lld:C0008525 a ncit:C7057 .
  
  dgn-gda:DGN9af5473d1e1e6f10057da92a834912b3 sio:SIO_000628 miriam-gene:10518, lld:C0008525;
    a sio:SIO_001121 .
}

dgn-np:NP233195.RA83m36ujC0ZgE3K_XkqcGQ74gC_flcTRaVXbII02-5i8130_provenance {
  dgn-np:NP233195.RA83m36ujC0ZgE3K_XkqcGQ74gC_flcTRaVXbII02-5i8130_assertion dcterms:description
      "[To assess the relative accuracy of p57(KIP2) immunostaining and molecular diagnosis by nuclear DNA microsatellite polymorphisms in discriminating CHM from its mimics, we analyzed archival tissue from 33 case patients (7 with a definitive diagnosis of CHM, 16 with a possible diagnosis of HM, and 10 with normal placentas) by both methods.]. 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:16949913;
    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:NP233195.RA83m36ujC0ZgE3K_XkqcGQ74gC_flcTRaVXbII02-5i8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:10+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" .
}