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http://rdf.disgenet.org/resource/nanopub/NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_head
{
this:
np:hasAssertion
dgn-np:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_assertion
a
np:Assertion
.
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a
np:Provenance
.
dgn-np:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_publicationInfo
a
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.
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dgn-np:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_assertion
{
miriam-gene:1861
a
ncit:C16612
.
lld:C0752203
a
ncit:C7057
.
dgn-gda:DGNcd29a7397e5158c92605602ea466b4a5
sio:SIO_000628
miriam-gene:1861
,
lld:C0752203
;
a
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.
}
dgn-np:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_provenance
{
dgn-np:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_assertion
dcterms:description
"[Overall, our findings do not support the hypothesis that common TOR1A variants affect susceptibility for sporadic primary dystonia, and that it is unlikely that common variants around the DYT genes confer substantial risk for sporadic primary dystonia.]. 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:22172551
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:54+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
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pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
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> , <
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
"v4.0.0.0" .
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pav:version
"v4.0.0" .
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