@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP53831.RA8Vfqpdsdy6JhBcVdRJ0NfCibh25fFl90H-NBvj1zScQ
> .
@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#
> .
dgn-np:NP53831.RA8Vfqpdsdy6JhBcVdRJ0NfCibh25fFl90H-NBvj1zScQ130_head
{
this:
np:hasAssertion
dgn-np:NP53831.RA8Vfqpdsdy6JhBcVdRJ0NfCibh25fFl90H-NBvj1zScQ130_assertion
;
np:hasProvenance
dgn-np:NP53831.RA8Vfqpdsdy6JhBcVdRJ0NfCibh25fFl90H-NBvj1zScQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP53831.RA8Vfqpdsdy6JhBcVdRJ0NfCibh25fFl90H-NBvj1zScQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP53831.RA8Vfqpdsdy6JhBcVdRJ0NfCibh25fFl90H-NBvj1zScQ130_assertion
a
np:Assertion
.
dgn-np:NP53831.RA8Vfqpdsdy6JhBcVdRJ0NfCibh25fFl90H-NBvj1zScQ130_provenance
a
np:Provenance
.
dgn-np:NP53831.RA8Vfqpdsdy6JhBcVdRJ0NfCibh25fFl90H-NBvj1zScQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP53831.RA8Vfqpdsdy6JhBcVdRJ0NfCibh25fFl90H-NBvj1zScQ130_assertion
{
miriam-gene:4843
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGNeaa4a92b6ab72223ab7d063530bf4ea2
sio:SIO_000628
miriam-gene:4843
,
lld:C0010054
;
a
sio:SIO_001122
.
}
dgn-np:NP53831.RA8Vfqpdsdy6JhBcVdRJ0NfCibh25fFl90H-NBvj1zScQ130_provenance
{
dgn-np:NP53831.RA8Vfqpdsdy6JhBcVdRJ0NfCibh25fFl90H-NBvj1zScQ130_assertion
dcterms:description
"[ It appears unlikely the R4/5 genotype plays a major role in the pathogenesis of CAD, as it was not associated with stenosis and atherosclerosis in RCA and LCX. However this genotype may have some role in more pronounced CAD, as seen in the LAD.]. 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:14636285
;
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:NP53831.RA8Vfqpdsdy6JhBcVdRJ0NfCibh25fFl90H-NBvj1zScQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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
pav:version
"v2.1.0" .
}