@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP563082.RALN3AFf6HREcx-2gTVv5_Yzk16k5a1WC5cnegpAuiVEc
> .
@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:NP563082.RALN3AFf6HREcx-2gTVv5_Yzk16k5a1WC5cnegpAuiVEc130_head
{
this:
np:hasAssertion
dgn-np:NP563082.RALN3AFf6HREcx-2gTVv5_Yzk16k5a1WC5cnegpAuiVEc130_assertion
;
np:hasProvenance
dgn-np:NP563082.RALN3AFf6HREcx-2gTVv5_Yzk16k5a1WC5cnegpAuiVEc130_provenance
;
np:hasPublicationInfo
dgn-np:NP563082.RALN3AFf6HREcx-2gTVv5_Yzk16k5a1WC5cnegpAuiVEc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP563082.RALN3AFf6HREcx-2gTVv5_Yzk16k5a1WC5cnegpAuiVEc130_assertion
a
np:Assertion
.
dgn-np:NP563082.RALN3AFf6HREcx-2gTVv5_Yzk16k5a1WC5cnegpAuiVEc130_provenance
a
np:Provenance
.
dgn-np:NP563082.RALN3AFf6HREcx-2gTVv5_Yzk16k5a1WC5cnegpAuiVEc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP563082.RALN3AFf6HREcx-2gTVv5_Yzk16k5a1WC5cnegpAuiVEc130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0002940
a
ncit:C7057
.
dgn-gda:DGN4546aebffeba6951163af4cc388520f5
sio:SIO_000628
miriam-gene:4846
,
lld:C0002940
;
a
sio:SIO_001121
.
}
dgn-np:NP563082.RALN3AFf6HREcx-2gTVv5_Yzk16k5a1WC5cnegpAuiVEc130_provenance
{
dgn-np:NP563082.RALN3AFf6HREcx-2gTVv5_Yzk16k5a1WC5cnegpAuiVEc130_assertion
dcterms:description
"[Based on recent studies supporting an increasingly relevant role for the critical vasomodulatory protein endothelial nitric oxide synthase (eNOS) in aneurysm pathobiology, the authors assayed blood from all 197 participants to determine and compare their eNOS genotypes.]. 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:15633984
;
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:NP563082.RALN3AFf6HREcx-2gTVv5_Yzk16k5a1WC5cnegpAuiVEc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:39+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" .
}