@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP827650.RAyRfUlwUJHY_kjQoSRMihu16G9t0qz1dtzcWQRHgS_QY> .
@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:NP827650.RAyRfUlwUJHY_kjQoSRMihu16G9t0qz1dtzcWQRHgS_QY130_head {
  this: np:hasAssertion dgn-np:NP827650.RAyRfUlwUJHY_kjQoSRMihu16G9t0qz1dtzcWQRHgS_QY130_assertion ;
    np:hasProvenance dgn-np:NP827650.RAyRfUlwUJHY_kjQoSRMihu16G9t0qz1dtzcWQRHgS_QY130_provenance ;
    np:hasPublicationInfo dgn-np:NP827650.RAyRfUlwUJHY_kjQoSRMihu16G9t0qz1dtzcWQRHgS_QY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP827650.RAyRfUlwUJHY_kjQoSRMihu16G9t0qz1dtzcWQRHgS_QY130_assertion a np:Assertion .
  dgn-np:NP827650.RAyRfUlwUJHY_kjQoSRMihu16G9t0qz1dtzcWQRHgS_QY130_provenance a np:Provenance .
  dgn-np:NP827650.RAyRfUlwUJHY_kjQoSRMihu16G9t0qz1dtzcWQRHgS_QY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP827650.RAyRfUlwUJHY_kjQoSRMihu16G9t0qz1dtzcWQRHgS_QY130_assertion {
  miriam-gene:1028 a ncit:C16612 .
  lld:C1456781 a ncit:C7057 .
  dgn-gda:DGN3c1197a3a280c6d94830e4810308c8a5 sio:SIO_000628 miriam-gene:1028 , lld:C1456781 ;
    a sio:SIO_001121 .
}
dgn-np:NP827650.RAyRfUlwUJHY_kjQoSRMihu16G9t0qz1dtzcWQRHgS_QY130_provenance {
  dgn-np:NP827650.RAyRfUlwUJHY_kjQoSRMihu16G9t0qz1dtzcWQRHgS_QY130_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:NP827650.RAyRfUlwUJHY_kjQoSRMihu16G9t0qz1dtzcWQRHgS_QY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:26+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> ;
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}