@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg
> .
@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 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#
> .
dgn-np:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_head
{
this:
np:hasAssertion
dgn-np:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_assertion
;
np:hasProvenance
dgn-np:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_provenance
;
np:hasPublicationInfo
dgn-np:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_assertion
a
np:Assertion
.
dgn-np:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_provenance
a
np:Provenance
.
dgn-np:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_assertion
{
miriam-gene:185
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGN18c731a1cf8626ca96cac29650e6d1ab
sio:SIO_000628
miriam-gene:185
,
lld:C1956346
;
a
sio:SIO_001122
.
}
dgn-np:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_provenance
{
dgn-np:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_assertion
dct:description
"[Six SNPs that were discovered and were associated with CAD may help in explaining the molecular basis of the disorder and the susceptibility to coronary atherosclerosis. It can also help identify early prediction, prevention and therapy for CAD.]. 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:21119571
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:22+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}