@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP805536.RAfwSVJJD5-vt053Hp6prwNEOK1DfNw3t6zeTNzga_gKM
> .
@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:NP805536.RAfwSVJJD5-vt053Hp6prwNEOK1DfNw3t6zeTNzga_gKM130_head
{
this:
np:hasAssertion
dgn-np:NP805536.RAfwSVJJD5-vt053Hp6prwNEOK1DfNw3t6zeTNzga_gKM130_assertion
;
np:hasProvenance
dgn-np:NP805536.RAfwSVJJD5-vt053Hp6prwNEOK1DfNw3t6zeTNzga_gKM130_provenance
;
np:hasPublicationInfo
dgn-np:NP805536.RAfwSVJJD5-vt053Hp6prwNEOK1DfNw3t6zeTNzga_gKM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP805536.RAfwSVJJD5-vt053Hp6prwNEOK1DfNw3t6zeTNzga_gKM130_assertion
a
np:Assertion
.
dgn-np:NP805536.RAfwSVJJD5-vt053Hp6prwNEOK1DfNw3t6zeTNzga_gKM130_provenance
a
np:Provenance
.
dgn-np:NP805536.RAfwSVJJD5-vt053Hp6prwNEOK1DfNw3t6zeTNzga_gKM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP805536.RAfwSVJJD5-vt053Hp6prwNEOK1DfNw3t6zeTNzga_gKM130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0042373
a
ncit:C7057
.
dgn-gda:DGN443d61bc26dcd6aa247be1714b520d09
sio:SIO_000628
miriam-gene:4846
,
lld:C0042373
;
a
sio:SIO_001121
.
}
dgn-np:NP805536.RAfwSVJJD5-vt053Hp6prwNEOK1DfNw3t6zeTNzga_gKM130_provenance
{
dgn-np:NP805536.RAfwSVJJD5-vt053Hp6prwNEOK1DfNw3t6zeTNzga_gKM130_assertion
dcterms:description
"[The association between the endothelial nitric oxide synthase (eNOS) gene with vascular diseases in Western populations and with severe preeclampsia (PE) in the Japanese population have been demonstrated, lacing the data in Chinese population.]. 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:17636229
;
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:NP805536.RAfwSVJJD5-vt053Hp6prwNEOK1DfNw3t6zeTNzga_gKM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:14+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" .
}