@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP173309.RAtUKK6k4Uld0OqGab8F0POP5eCnCq72aw4XABGlAZj3w> .
@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:NP173309.RAtUKK6k4Uld0OqGab8F0POP5eCnCq72aw4XABGlAZj3w130_head {
  this: np:hasAssertion dgn-np:NP173309.RAtUKK6k4Uld0OqGab8F0POP5eCnCq72aw4XABGlAZj3w130_assertion;
    np:hasProvenance dgn-np:NP173309.RAtUKK6k4Uld0OqGab8F0POP5eCnCq72aw4XABGlAZj3w130_provenance;
    np:hasPublicationInfo dgn-np:NP173309.RAtUKK6k4Uld0OqGab8F0POP5eCnCq72aw4XABGlAZj3w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP173309.RAtUKK6k4Uld0OqGab8F0POP5eCnCq72aw4XABGlAZj3w130_assertion a np:Assertion .
  
  dgn-np:NP173309.RAtUKK6k4Uld0OqGab8F0POP5eCnCq72aw4XABGlAZj3w130_provenance a np:Provenance .
  
  dgn-np:NP173309.RAtUKK6k4Uld0OqGab8F0POP5eCnCq72aw4XABGlAZj3w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP173309.RAtUKK6k4Uld0OqGab8F0POP5eCnCq72aw4XABGlAZj3w130_assertion {
  miriam-gene:10518 a ncit:C16612 .
  
  lld:C0020217 a ncit:C7057 .
  
  dgn-gda:DGN728c3f8388d20d717cf52d47df3b68fc sio:SIO_000628 miriam-gene:10518, lld:C0020217;
    a sio:SIO_001121 .
}

dgn-np:NP173309.RAtUKK6k4Uld0OqGab8F0POP5eCnCq72aw4XABGlAZj3w130_provenance {
  dgn-np:NP173309.RAtUKK6k4Uld0OqGab8F0POP5eCnCq72aw4XABGlAZj3w130_assertion dcterms:description
      "[Pathological review and genotyping of other molar pregnancies in these cases showed them to be typical CHM with negative p57(KIP2) immunostaining of the cytotrophoblast cells and villous stroma and to be diploid but biparental, confirming a diagnosis of familial recurrent hydatidiform mole (FRHM).]. 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:23125094;
    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:NP173309.RAtUKK6k4Uld0OqGab8F0POP5eCnCq72aw4XABGlAZj3w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:33+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" .
}