@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP252973.RAPywL_RAF_fjHa3zRwNijF5qwC0AOHbNx7Mh-ZCIu-KY
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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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#
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP252973.RAPywL_RAF_fjHa3zRwNijF5qwC0AOHbNx7Mh-ZCIu-KY130_assertion
;
np:hasProvenance
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np:Nanopublication
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a
np:Assertion
.
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a
np:Provenance
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.
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{
miriam-gene:54551
a
ncit:C16612
.
lld:C0432072
a
ncit:C7057
.
dgn-gda:DGN1684ca9430b9f8847a24c8b3f6e25682
sio:SIO_000628
miriam-gene:54551
,
lld:C0432072
;
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.
}
dgn-np:NP252973.RAPywL_RAF_fjHa3zRwNijF5qwC0AOHbNx7Mh-ZCIu-KY130_provenance
{
dgn-np:NP252973.RAPywL_RAF_fjHa3zRwNijF5qwC0AOHbNx7Mh-ZCIu-KY130_assertion
dcterms:description
"[We hypothesize that, although loss of necdin expression may be important in the neonatal presentation of PWS, loss of MAGEL2 may be critical to abnormalities in brain development and dysmorphic features in individuals with PWS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:10915770
;
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:NP252973.RAPywL_RAF_fjHa3zRwNijF5qwC0AOHbNx7Mh-ZCIu-KY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:21+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:createdBy
<
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pav:version
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