@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP354384.RAfznaq3OYQLsnmPUFLUN0c3s7EIY0MwRXsHO8psFRRDw> .
@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:NP354384.RAfznaq3OYQLsnmPUFLUN0c3s7EIY0MwRXsHO8psFRRDw130_head {
  this: np:hasAssertion dgn-np:NP354384.RAfznaq3OYQLsnmPUFLUN0c3s7EIY0MwRXsHO8psFRRDw130_assertion ;
    np:hasProvenance dgn-np:NP354384.RAfznaq3OYQLsnmPUFLUN0c3s7EIY0MwRXsHO8psFRRDw130_provenance ;
    np:hasPublicationInfo dgn-np:NP354384.RAfznaq3OYQLsnmPUFLUN0c3s7EIY0MwRXsHO8psFRRDw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP354384.RAfznaq3OYQLsnmPUFLUN0c3s7EIY0MwRXsHO8psFRRDw130_assertion a np:Assertion .
  dgn-np:NP354384.RAfznaq3OYQLsnmPUFLUN0c3s7EIY0MwRXsHO8psFRRDw130_provenance a np:Provenance .
  dgn-np:NP354384.RAfznaq3OYQLsnmPUFLUN0c3s7EIY0MwRXsHO8psFRRDw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP354384.RAfznaq3OYQLsnmPUFLUN0c3s7EIY0MwRXsHO8psFRRDw130_assertion {
  miriam-gene:1028 a ncit:C16612 .
  lld:C0027962 a ncit:C7057 .
  dgn-gda:DGN0d03c08d974c2e3cbd6754e6d4450677 sio:SIO_000628 miriam-gene:1028 , lld:C0027962 ;
    a sio:SIO_001121 .
}
dgn-np:NP354384.RAfznaq3OYQLsnmPUFLUN0c3s7EIY0MwRXsHO8psFRRDw130_provenance {
  dgn-np:NP354384.RAfznaq3OYQLsnmPUFLUN0c3s7EIY0MwRXsHO8psFRRDw130_assertion dcterms:description "[In all cases, the pathologic diagnoses were easily resolved: two cases were partial moles (triploid, p57 positive), two cases were early complete moles (diploid, p57 negative), and two cases were twin gestations with normal villi (diploid, p57 positive) admixed with villi from a complete hydatidiform mole (diploid, p57 negative).]. 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:12063872 ;
    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:NP354384.RAfznaq3OYQLsnmPUFLUN0c3s7EIY0MwRXsHO8psFRRDw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:28+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" .
}