@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP835076.RALdDDxiEdw_yWLLgPUw-bQPP5qJbsWxTFPvflRREe0HY
> .
@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/v3.0.0/void/
> .
dgn-np:NP835076.RALdDDxiEdw_yWLLgPUw-bQPP5qJbsWxTFPvflRREe0HY130_head
{
this:
np:hasAssertion
dgn-np:NP835076.RALdDDxiEdw_yWLLgPUw-bQPP5qJbsWxTFPvflRREe0HY130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP835076.RALdDDxiEdw_yWLLgPUw-bQPP5qJbsWxTFPvflRREe0HY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP835076.RALdDDxiEdw_yWLLgPUw-bQPP5qJbsWxTFPvflRREe0HY130_assertion
a
np:Assertion
.
dgn-np:NP835076.RALdDDxiEdw_yWLLgPUw-bQPP5qJbsWxTFPvflRREe0HY130_provenance
a
np:Provenance
.
dgn-np:NP835076.RALdDDxiEdw_yWLLgPUw-bQPP5qJbsWxTFPvflRREe0HY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP835076.RALdDDxiEdw_yWLLgPUw-bQPP5qJbsWxTFPvflRREe0HY130_assertion
{
miriam-gene:10019
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGNe2a314792f0f5b1340350d91de2b05e3
sio:SIO_000628
miriam-gene:10019
,
lld:C0010068
;
a
sio:SIO_001122
.
}
dgn-np:NP835076.RALdDDxiEdw_yWLLgPUw-bQPP5qJbsWxTFPvflRREe0HY130_provenance
{
dgn-np:NP835076.RALdDDxiEdw_yWLLgPUw-bQPP5qJbsWxTFPvflRREe0HY130_assertion
dcterms:description
"[In conclusion, our results supported a significant association between rs3184504 of SH2B3 gene and the risk of CHD in Europeans and South Asians, although we were unable to observe association between the four variants and the risk of CHD in Han Chinese.]. 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:23328882
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP835076.RALdDDxiEdw_yWLLgPUw-bQPP5qJbsWxTFPvflRREe0HY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:07+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}