@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP208457.RAo-w37fEXA4IXSR2Sa9V0H5wF2Mu9fq1oe2YjkkQPA6U> .
@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:NP208457.RAo-w37fEXA4IXSR2Sa9V0H5wF2Mu9fq1oe2YjkkQPA6U130_head {
  this: np:hasAssertion dgn-np:NP208457.RAo-w37fEXA4IXSR2Sa9V0H5wF2Mu9fq1oe2YjkkQPA6U130_assertion ;
    np:hasProvenance dgn-np:NP208457.RAo-w37fEXA4IXSR2Sa9V0H5wF2Mu9fq1oe2YjkkQPA6U130_provenance ;
    np:hasPublicationInfo dgn-np:NP208457.RAo-w37fEXA4IXSR2Sa9V0H5wF2Mu9fq1oe2YjkkQPA6U130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP208457.RAo-w37fEXA4IXSR2Sa9V0H5wF2Mu9fq1oe2YjkkQPA6U130_assertion a np:Assertion .
  dgn-np:NP208457.RAo-w37fEXA4IXSR2Sa9V0H5wF2Mu9fq1oe2YjkkQPA6U130_provenance a np:Provenance .
  dgn-np:NP208457.RAo-w37fEXA4IXSR2Sa9V0H5wF2Mu9fq1oe2YjkkQPA6U130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP208457.RAo-w37fEXA4IXSR2Sa9V0H5wF2Mu9fq1oe2YjkkQPA6U130_assertion {
  miriam-gene:2562 a ncit:C16612 .
  lld:C0162635 a ncit:C7057 .
  dgn-gda:DGN7179251a0bd6ddfbea5a9c9b92ceb8c8 sio:SIO_000628 miriam-gene:2562 , lld:C0162635 ;
    a sio:SIO_001121 .
}
dgn-np:NP208457.RAo-w37fEXA4IXSR2Sa9V0H5wF2Mu9fq1oe2YjkkQPA6U130_provenance {
  dgn-np:NP208457.RAo-w37fEXA4IXSR2Sa9V0H5wF2Mu9fq1oe2YjkkQPA6U130_assertion dcterms:description "[Clinical reassessment and the use of molecular studies, including methylation analysis with an SNRPN probe, microsatellite analyses of D15S11, GABRB3 and D15S113 loci, and fluorescence in situ hybridization (FISH) using the SNRPN and GABRB3 probes, are consistent with a diagnosis of Angelman syndrome (AS) due to paternal isodisomy.]. 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:9831341 ;
    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:NP208457.RAo-w37fEXA4IXSR2Sa9V0H5wF2Mu9fq1oe2YjkkQPA6U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:55+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" .
}