@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47458.RAJdtmKWfUgRhd2ENK388E4h7sXtW4FR2pjMM8ccDpz9g
> .
@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:NP47458.RAJdtmKWfUgRhd2ENK388E4h7sXtW4FR2pjMM8ccDpz9g130_head
{
this:
np:hasAssertion
dgn-np:NP47458.RAJdtmKWfUgRhd2ENK388E4h7sXtW4FR2pjMM8ccDpz9g130_assertion
;
np:hasProvenance
dgn-np:NP47458.RAJdtmKWfUgRhd2ENK388E4h7sXtW4FR2pjMM8ccDpz9g130_provenance
;
np:hasPublicationInfo
dgn-np:NP47458.RAJdtmKWfUgRhd2ENK388E4h7sXtW4FR2pjMM8ccDpz9g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47458.RAJdtmKWfUgRhd2ENK388E4h7sXtW4FR2pjMM8ccDpz9g130_assertion
a
np:Assertion
.
dgn-np:NP47458.RAJdtmKWfUgRhd2ENK388E4h7sXtW4FR2pjMM8ccDpz9g130_provenance
a
np:Provenance
.
dgn-np:NP47458.RAJdtmKWfUgRhd2ENK388E4h7sXtW4FR2pjMM8ccDpz9g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47458.RAJdtmKWfUgRhd2ENK388E4h7sXtW4FR2pjMM8ccDpz9g130_assertion
{
miriam-gene:6356
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGN235f043f29d88d1c407ff83f53169fb3
sio:SIO_000628
miriam-gene:6356
,
lld:C0027051
;
a
sio:SIO_001122
.
}
dgn-np:NP47458.RAJdtmKWfUgRhd2ENK388E4h7sXtW4FR2pjMM8ccDpz9g130_provenance
{
dgn-np:NP47458.RAJdtmKWfUgRhd2ENK388E4h7sXtW4FR2pjMM8ccDpz9g130_assertion
dcterms:description
"[In this cohort, a T for A substitution at amino acid 23 in the eotaxin gene is associated with increased risk for incident myocardial infarction. If confirmed in other cohorts, these data support the emerging hypothesis that eotaxin participates in atherosclerosis.]. 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:15186951
;
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:NP47458.RAJdtmKWfUgRhd2ENK388E4h7sXtW4FR2pjMM8ccDpz9g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}