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http://rdf.disgenet.org/nanopublications.trig#NP263098.RAAHlO5sVUWyLIL-r-PEq9wWOibbShE3U1TOnEgZWfLfU
> .
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> .
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http://www.w3.org/2001/XMLSchema#
> .
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http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
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http://identifiers.org/pubmed/
> .
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http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
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np:hasProvenance
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a
np:Assertion
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a
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{
miriam-gene:8926
a
ncit:C16612
.
lld:C0032897
a
ncit:C7057
.
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dgn-np:NP263098.RAAHlO5sVUWyLIL-r-PEq9wWOibbShE3U1TOnEgZWfLfU130_assertion
dcterms:description
"[Nine probands with a firm clinical diagnosis of PWS but who had neither a typical deletion in the PWS region nor UPD(15)mat were investigated for inactivating mutations in 11 genes located in the PWS region, including SNURF and SNRPN, which are associated with the imprinting centre.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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miriam-pubmed:17262171
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eco:ECO_0000203
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pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
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;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
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xsd:dateTime
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dcterms:rights
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> ;
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