@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP601529.RAOyGEjvCUyCjpAN3IQOqBubMWleNUJ4Fz9pCX8Wp5hXM> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP601529.RAOyGEjvCUyCjpAN3IQOqBubMWleNUJ4Fz9pCX8Wp5hXM130_head {
   this: np:hasAssertion dgn-np:NP601529.RAOyGEjvCUyCjpAN3IQOqBubMWleNUJ4Fz9pCX8Wp5hXM130_assertion ;
    np:hasProvenance dgn-np:NP601529.RAOyGEjvCUyCjpAN3IQOqBubMWleNUJ4Fz9pCX8Wp5hXM130_provenance ;
    np:hasPublicationInfo dgn-np:NP601529.RAOyGEjvCUyCjpAN3IQOqBubMWleNUJ4Fz9pCX8Wp5hXM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP601529.RAOyGEjvCUyCjpAN3IQOqBubMWleNUJ4Fz9pCX8Wp5hXM130_assertion a np:Assertion .
  dgn-np:NP601529.RAOyGEjvCUyCjpAN3IQOqBubMWleNUJ4Fz9pCX8Wp5hXM130_provenance a np:Provenance .
  dgn-np:NP601529.RAOyGEjvCUyCjpAN3IQOqBubMWleNUJ4Fz9pCX8Wp5hXM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP601529.RAOyGEjvCUyCjpAN3IQOqBubMWleNUJ4Fz9pCX8Wp5hXM130_assertion {
   miriam-gene:4948 a ncit:C16612 .
  lld:C0162835 a ncit:C7057 .
  dgn-gda:DGN8570d75bbf7c511a932088f75ca45ff9 sio:SIO_000628 miriam-gene:4948 , lld:C0162835 ;
    a sio:SIO_001121 .
}
dgn-np:NP601529.RAOyGEjvCUyCjpAN3IQOqBubMWleNUJ4Fz9pCX8Wp5hXM130_provenance {
   dgn-np:NP601529.RAOyGEjvCUyCjpAN3IQOqBubMWleNUJ4Fz9pCX8Wp5hXM130_assertion dcterms:description "[Cases of PWS due to UPD do not appear to differ from those due to deletion (hypopigmentation in deletional cases can be explained by loss of D15S12 downstream from the critical region).]. 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:8872029 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP601529.RAOyGEjvCUyCjpAN3IQOqBubMWleNUJ4Fz9pCX8Wp5hXM130_publicationInfo {
   this: dcterms:created "2015-08-25T14:43:39+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}