@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP61776.RAK5cJ5l6sSunXvCKRdJGnW3hS4NQDJg4XJYQ8agCrOLc
> .
@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:NP61776.RAK5cJ5l6sSunXvCKRdJGnW3hS4NQDJg4XJYQ8agCrOLc130_head
{
this:
np:hasAssertion
dgn-np:NP61776.RAK5cJ5l6sSunXvCKRdJGnW3hS4NQDJg4XJYQ8agCrOLc130_assertion
;
np:hasProvenance
dgn-np:NP61776.RAK5cJ5l6sSunXvCKRdJGnW3hS4NQDJg4XJYQ8agCrOLc130_provenance
;
np:hasPublicationInfo
dgn-np:NP61776.RAK5cJ5l6sSunXvCKRdJGnW3hS4NQDJg4XJYQ8agCrOLc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP61776.RAK5cJ5l6sSunXvCKRdJGnW3hS4NQDJg4XJYQ8agCrOLc130_assertion
a
np:Assertion
.
dgn-np:NP61776.RAK5cJ5l6sSunXvCKRdJGnW3hS4NQDJg4XJYQ8agCrOLc130_provenance
a
np:Provenance
.
dgn-np:NP61776.RAK5cJ5l6sSunXvCKRdJGnW3hS4NQDJg4XJYQ8agCrOLc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP61776.RAK5cJ5l6sSunXvCKRdJGnW3hS4NQDJg4XJYQ8agCrOLc130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0038525
a
ncit:C7057
.
dgn-gda:DGN5b081789b43bf36f5bb00a3983e39f39
sio:SIO_000628
miriam-gene:4846
,
lld:C0038525
;
a
sio:SIO_001122
.
}
dgn-np:NP61776.RAK5cJ5l6sSunXvCKRdJGnW3hS4NQDJg4XJYQ8agCrOLc130_provenance
{
dgn-np:NP61776.RAK5cJ5l6sSunXvCKRdJGnW3hS4NQDJg4XJYQ8agCrOLc130_assertion
dcterms:description
"[ The eNOS T-786C SNP distinguishes genetically between small and large ruptured aneurysms. Although not predictive of SAH in the population at large, our data suggest that among persons with known intracranial aneurysms, eNOS T-786C genotype may be a factor influencing the size at which an aneurysm ruptures, a finding that should be taken into consideration along with other anatomic features of the aneurysm.]. 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:14576373
;
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:NP61776.RAK5cJ5l6sSunXvCKRdJGnW3hS4NQDJg4XJYQ8agCrOLc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}