@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP861443.RArbtBR0FPh4DsDY0AUAN3cpOTzkd-0xMUK3qvogilaYU
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP861443.RArbtBR0FPh4DsDY0AUAN3cpOTzkd-0xMUK3qvogilaYU130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP861443.RArbtBR0FPh4DsDY0AUAN3cpOTzkd-0xMUK3qvogilaYU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP861443.RArbtBR0FPh4DsDY0AUAN3cpOTzkd-0xMUK3qvogilaYU130_assertion
a
np:Assertion
.
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a
np:Provenance
.
dgn-np:NP861443.RArbtBR0FPh4DsDY0AUAN3cpOTzkd-0xMUK3qvogilaYU130_publicationInfo
a
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.
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dgn-np:NP861443.RArbtBR0FPh4DsDY0AUAN3cpOTzkd-0xMUK3qvogilaYU130_assertion
{
miriam-gene:11173
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN62d11b7609cf135236f11e68fdef19e9
sio:SIO_000628
miriam-gene:11173
,
lld:C0010054
;
a
sio:SIO_001122
.
}
dgn-np:NP861443.RArbtBR0FPh4DsDY0AUAN3cpOTzkd-0xMUK3qvogilaYU130_provenance
{
dgn-np:NP861443.RArbtBR0FPh4DsDY0AUAN3cpOTzkd-0xMUK3qvogilaYU130_assertion
dcterms:description
"[Recent studies have identified the ABO rs579459, PPAP2B rs17114036, and ADAMTS7 rs3825807 polymorphisms as genetic variants associated with coronary artery disease and the PIK3CG rs17398575 and EDNRA rs1878406 polymorphisms as the most significant signals related to the presence of carotid plaque in nonrheumatic Caucasian individuals.]. 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:24795506
;
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:NP861443.RArbtBR0FPh4DsDY0AUAN3cpOTzkd-0xMUK3qvogilaYU130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:23+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: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
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"v3.0.0" .
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