@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44799.RA4VFUSJY886lhLjE2V-8hQd19tDRPXMoIwSyyGlc9lCs
> .
@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:NP44799.RA4VFUSJY886lhLjE2V-8hQd19tDRPXMoIwSyyGlc9lCs130_head
{
this:
np:hasAssertion
dgn-np:NP44799.RA4VFUSJY886lhLjE2V-8hQd19tDRPXMoIwSyyGlc9lCs130_assertion
;
np:hasProvenance
dgn-np:NP44799.RA4VFUSJY886lhLjE2V-8hQd19tDRPXMoIwSyyGlc9lCs130_provenance
;
np:hasPublicationInfo
dgn-np:NP44799.RA4VFUSJY886lhLjE2V-8hQd19tDRPXMoIwSyyGlc9lCs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44799.RA4VFUSJY886lhLjE2V-8hQd19tDRPXMoIwSyyGlc9lCs130_assertion
a
np:Assertion
.
dgn-np:NP44799.RA4VFUSJY886lhLjE2V-8hQd19tDRPXMoIwSyyGlc9lCs130_provenance
a
np:Provenance
.
dgn-np:NP44799.RA4VFUSJY886lhLjE2V-8hQd19tDRPXMoIwSyyGlc9lCs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44799.RA4VFUSJY886lhLjE2V-8hQd19tDRPXMoIwSyyGlc9lCs130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGN4fbf11aed1de426541a15af2482d28b2
sio:SIO_000628
miriam-gene:2099
,
lld:C1956346
;
a
sio:SIO_001122
.
}
dgn-np:NP44799.RA4VFUSJY886lhLjE2V-8hQd19tDRPXMoIwSyyGlc9lCs130_provenance
{
dgn-np:NP44799.RA4VFUSJY886lhLjE2V-8hQd19tDRPXMoIwSyyGlc9lCs130_assertion
dcterms:description
"[These data suggest that the improvement in endothelium-dependent dilation and the reduction in perfusion abnormalities by increasing estradiol levels with HRT in postmenopausal women with coronary artery disease may differ with respect to different genotypes, the effect being more prominent in those patients with ER-alpha IVS1-397 CC genotype.]. 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:16612068
;
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:NP44799.RA4VFUSJY886lhLjE2V-8hQd19tDRPXMoIwSyyGlc9lCs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}