@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP393678.RASXQ12dMA1YNT83rLibbe_c5ZWsmVB384k3VZOpa9ZFs
> .
@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:NP393678.RASXQ12dMA1YNT83rLibbe_c5ZWsmVB384k3VZOpa9ZFs130_head
{
this:
np:hasAssertion
dgn-np:NP393678.RASXQ12dMA1YNT83rLibbe_c5ZWsmVB384k3VZOpa9ZFs130_assertion
;
np:hasProvenance
dgn-np:NP393678.RASXQ12dMA1YNT83rLibbe_c5ZWsmVB384k3VZOpa9ZFs130_provenance
;
np:hasPublicationInfo
dgn-np:NP393678.RASXQ12dMA1YNT83rLibbe_c5ZWsmVB384k3VZOpa9ZFs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP393678.RASXQ12dMA1YNT83rLibbe_c5ZWsmVB384k3VZOpa9ZFs130_assertion
a
np:Assertion
.
dgn-np:NP393678.RASXQ12dMA1YNT83rLibbe_c5ZWsmVB384k3VZOpa9ZFs130_provenance
a
np:Provenance
.
dgn-np:NP393678.RASXQ12dMA1YNT83rLibbe_c5ZWsmVB384k3VZOpa9ZFs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP393678.RASXQ12dMA1YNT83rLibbe_c5ZWsmVB384k3VZOpa9ZFs130_assertion
{
miriam-gene:1666
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN5eaae4a1f64ad8403cbfd255dad9f2ad
sio:SIO_000628
miriam-gene:1666
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP393678.RASXQ12dMA1YNT83rLibbe_c5ZWsmVB384k3VZOpa9ZFs130_provenance
{
dgn-np:NP393678.RASXQ12dMA1YNT83rLibbe_c5ZWsmVB384k3VZOpa9ZFs130_assertion
dcterms:description
"[Common genetic polymorphisms within the promoter and exonic sequences of CYBA, the gene that encodes the p22phox subunit of the NADPH oxidase, have been characterized in the context of cardiovascular diseases.]. 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:20603655
;
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:NP393678.RASXQ12dMA1YNT83rLibbe_c5ZWsmVB384k3VZOpa9ZFs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:54+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" .
}