@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE
> .
@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:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_head
{
this:
np:hasAssertion
dgn-np:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_assertion
;
np:hasProvenance
dgn-np:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_provenance
;
np:hasPublicationInfo
dgn-np:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_assertion
a
np:Assertion
.
dgn-np:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_provenance
a
np:Provenance
.
dgn-np:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_assertion
{
miriam-gene:2053
a
ncit:C16612
.
lld:C3272363
a
ncit:C7057
.
dgn-gda:DGN861033ca0b34269daebf75a384d25b1e
sio:SIO_000628
miriam-gene:2053
,
lld:C3272363
;
a
sio:SIO_001121
.
}
dgn-np:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_provenance
{
dgn-np:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_assertion
dcterms:description
"[This suggests that the relationship between the EPHX2 gene and risk of ischemic stroke and other cardiovascular disease does not exist or its effect size is likely to be quite small.]. 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:19940276
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP575713.RAjH0f0706PXXVReTMa_3TrdaBNqh3HKZNOkPvnt-DmnE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:47+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" .
}