@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP594182.RAcXs3kot5DpbtQ3IwjYODdB1LeDVN1C6wp4oXzFQtcME
> .
@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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{
this:
np:hasAssertion
dgn-np:NP594182.RAcXs3kot5DpbtQ3IwjYODdB1LeDVN1C6wp4oXzFQtcME130_assertion
;
np:hasProvenance
dgn-np:NP594182.RAcXs3kot5DpbtQ3IwjYODdB1LeDVN1C6wp4oXzFQtcME130_provenance
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np:hasPublicationInfo
dgn-np:NP594182.RAcXs3kot5DpbtQ3IwjYODdB1LeDVN1C6wp4oXzFQtcME130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP594182.RAcXs3kot5DpbtQ3IwjYODdB1LeDVN1C6wp4oXzFQtcME130_assertion
a
np:Assertion
.
dgn-np:NP594182.RAcXs3kot5DpbtQ3IwjYODdB1LeDVN1C6wp4oXzFQtcME130_provenance
a
np:Provenance
.
dgn-np:NP594182.RAcXs3kot5DpbtQ3IwjYODdB1LeDVN1C6wp4oXzFQtcME130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP594182.RAcXs3kot5DpbtQ3IwjYODdB1LeDVN1C6wp4oXzFQtcME130_assertion
{
miriam-gene:6311
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGN292866db077889e5558841d43b43aed1
sio:SIO_000628
miriam-gene:6311
,
lld:C0028754
;
a
sio:SIO_001121
.
}
dgn-np:NP594182.RAcXs3kot5DpbtQ3IwjYODdB1LeDVN1C6wp4oXzFQtcME130_provenance
{
dgn-np:NP594182.RAcXs3kot5DpbtQ3IwjYODdB1LeDVN1C6wp4oXzFQtcME130_assertion
dcterms:description
"[Although we did not identify variants leading to novel amino acid substitutions, nonsense or frameshift mutations, this study warrants further examination of variation in the ATXN2 gene in obesity and related phenotypes in a larger case-control study with emphasis on rs695872 and CAG repeat structure.]. 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:20016785
;
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:NP594182.RAcXs3kot5DpbtQ3IwjYODdB1LeDVN1C6wp4oXzFQtcME130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:57+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
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"v2.1.0" .
}