@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4> .
@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:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_head {
  this: np:hasAssertion dgn-np:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_assertion ;
    np:hasProvenance dgn-np:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_provenance ;
    np:hasPublicationInfo dgn-np:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_assertion a np:Assertion .
  dgn-np:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_provenance a np:Provenance .
  dgn-np:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_assertion {
  miriam-gene:7389 a ncit:C16612 .
  lld:C0162835 a ncit:C7057 .
  dgn-gda:DGNa6283c23141b95e3c10c70f9420f01de sio:SIO_000628 miriam-gene:7389 , lld:C0162835 ;
    a sio:SIO_001121 .
}
dgn-np:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_provenance {
  dgn-np:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_assertion dcterms:description "[In addition to a higher frequency of hypopigmentation among deletion patients, minor phenotypic differences between deletion and UPD patients have recently been reported, including lower birth weight in the deletion group, shorter birth length in males with UPD, and shorter course of gavage feeding and later onset of hyperphagia in females with UPD.]. 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:9215778 ;
    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:NP352225.RADa4AaoGEqIhZ9qttvEls_0RRgf9svi-qZEkTCeQM6C4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:27+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" .
}