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http://rdf.disgenet.org/nanopublications.trig#NP483974.RAHEqvr6OgdG8C7Q0Hdgy8qgzbgC_S6LmrA2r8Qqj9cIE
> .
@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#
> .
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{
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np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP483974.RAHEqvr6OgdG8C7Q0Hdgy8qgzbgC_S6LmrA2r8Qqj9cIE130_provenance
a
np:Provenance
.
dgn-np:NP483974.RAHEqvr6OgdG8C7Q0Hdgy8qgzbgC_S6LmrA2r8Qqj9cIE130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:9569
a
ncit:C16612
.
lld:C0175702
a
ncit:C7057
.
dgn-gda:DGN1810b21f7f68b10b4eb111fe23b83100
sio:SIO_000628
miriam-gene:9569
,
lld:C0175702
;
a
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.
}
dgn-np:NP483974.RAHEqvr6OgdG8C7Q0Hdgy8qgzbgC_S6LmrA2r8Qqj9cIE130_provenance
{
dgn-np:NP483974.RAHEqvr6OgdG8C7Q0Hdgy8qgzbgC_S6LmrA2r8Qqj9cIE130_assertion
dcterms:description
"[These results combine with previous data from small deletions to suggest the gene GTF2IRD1 is associated with WS facies and VSC, and that GTF2I may contribute to WS social behaviors including increased gaze and attention to strangers.]. 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:19205026
;
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 .
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dgn-np:NP483974.RAHEqvr6OgdG8C7Q0Hdgy8qgzbgC_S6LmrA2r8Qqj9cIE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:49+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
<
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> , <
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> , <
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> ;
pav:createdBy
<
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pav:version
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dgn-void:disgenetrdf
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"v2.1.0" .
}