@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP598230.RALfcCTsxoCBpc3c52cv6OYe3PI0PXCjDMawV2BWyaE-I
> .
@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:NP598230.RALfcCTsxoCBpc3c52cv6OYe3PI0PXCjDMawV2BWyaE-I130_head
{
this:
np:hasAssertion
dgn-np:NP598230.RALfcCTsxoCBpc3c52cv6OYe3PI0PXCjDMawV2BWyaE-I130_assertion
;
np:hasProvenance
dgn-np:NP598230.RALfcCTsxoCBpc3c52cv6OYe3PI0PXCjDMawV2BWyaE-I130_provenance
;
np:hasPublicationInfo
dgn-np:NP598230.RALfcCTsxoCBpc3c52cv6OYe3PI0PXCjDMawV2BWyaE-I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP598230.RALfcCTsxoCBpc3c52cv6OYe3PI0PXCjDMawV2BWyaE-I130_assertion
a
np:Assertion
.
dgn-np:NP598230.RALfcCTsxoCBpc3c52cv6OYe3PI0PXCjDMawV2BWyaE-I130_provenance
a
np:Provenance
.
dgn-np:NP598230.RALfcCTsxoCBpc3c52cv6OYe3PI0PXCjDMawV2BWyaE-I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP598230.RALfcCTsxoCBpc3c52cv6OYe3PI0PXCjDMawV2BWyaE-I130_assertion
{
miriam-gene:342977
a
ncit:C16612
.
lld:C0018799
a
ncit:C7057
.
dgn-gda:DGN7e3bef6b59c641559a7623e5a9ea60bc
sio:SIO_000628
miriam-gene:342977
,
lld:C0018799
;
a
sio:SIO_001121
.
}
dgn-np:NP598230.RALfcCTsxoCBpc3c52cv6OYe3PI0PXCjDMawV2BWyaE-I130_provenance
{
dgn-np:NP598230.RALfcCTsxoCBpc3c52cv6OYe3PI0PXCjDMawV2BWyaE-I130_assertion
dcterms:description
"[The NOS3 -786 T/C (SNP id rs2070744; http://www.ensembl.org ), intron 4 variable number tandem repeat (VNTR), and Glu298Asp (SNP id rs1799983) polymorphisms, have been associated with differences in NO plasma concentrations and with the risk of hypertension (HT) and ischemic cardiac disease.]. 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:21293869
;
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:NP598230.RALfcCTsxoCBpc3c52cv6OYe3PI0PXCjDMawV2BWyaE-I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:59+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" .
}