@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP594519.RAi7EvBRS9rszCdEkQPrJoJjP6KM0WQ63l6lnJLGM3XqY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP594519.RAi7EvBRS9rszCdEkQPrJoJjP6KM0WQ63l6lnJLGM3XqY130_head
{
this:
np:hasAssertion
dgn-np:NP594519.RAi7EvBRS9rszCdEkQPrJoJjP6KM0WQ63l6lnJLGM3XqY130_assertion
;
np:hasProvenance
dgn-np:NP594519.RAi7EvBRS9rszCdEkQPrJoJjP6KM0WQ63l6lnJLGM3XqY130_provenance
;
np:hasPublicationInfo
dgn-np:NP594519.RAi7EvBRS9rszCdEkQPrJoJjP6KM0WQ63l6lnJLGM3XqY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP594519.RAi7EvBRS9rszCdEkQPrJoJjP6KM0WQ63l6lnJLGM3XqY130_assertion
a
np:Assertion
.
dgn-np:NP594519.RAi7EvBRS9rszCdEkQPrJoJjP6KM0WQ63l6lnJLGM3XqY130_provenance
a
np:Provenance
.
dgn-np:NP594519.RAi7EvBRS9rszCdEkQPrJoJjP6KM0WQ63l6lnJLGM3XqY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP594519.RAi7EvBRS9rszCdEkQPrJoJjP6KM0WQ63l6lnJLGM3XqY130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0036421
a
ncit:C7057
.
dgn-gda:DGNe1719dbf08af7f51ba70b452ffb5f591
sio:SIO_000628
miriam-gene:4846
,
lld:C0036421
;
a
sio:SIO_001122
.
}
dgn-np:NP594519.RAi7EvBRS9rszCdEkQPrJoJjP6KM0WQ63l6lnJLGM3XqY130_provenance
{
dgn-np:NP594519.RAi7EvBRS9rszCdEkQPrJoJjP6KM0WQ63l6lnJLGM3XqY130_assertion
dcterms:description
"[We investigated haemorheological variables in patients with idiopathic sudden sensorineural hearing loss (ISSHL), retinal vein occlusion (RVO) and systemic sclerosis (SSc), as possible models of microvascular damage, and their relationship with eNOS gene T-786C, G894T and 4a/4b polymorphisms.]. 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:17634663
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP594519.RAi7EvBRS9rszCdEkQPrJoJjP6KM0WQ63l6lnJLGM3XqY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:35+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}