@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP883704.RAKY-O0YJXRRw9C9QPJLOrh5suQvKilW7Nphe_c8vrWR8
> .
@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:NP883704.RAKY-O0YJXRRw9C9QPJLOrh5suQvKilW7Nphe_c8vrWR8130_head
{
this:
np:hasAssertion
dgn-np:NP883704.RAKY-O0YJXRRw9C9QPJLOrh5suQvKilW7Nphe_c8vrWR8130_assertion
;
np:hasProvenance
dgn-np:NP883704.RAKY-O0YJXRRw9C9QPJLOrh5suQvKilW7Nphe_c8vrWR8130_provenance
;
np:hasPublicationInfo
dgn-np:NP883704.RAKY-O0YJXRRw9C9QPJLOrh5suQvKilW7Nphe_c8vrWR8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP883704.RAKY-O0YJXRRw9C9QPJLOrh5suQvKilW7Nphe_c8vrWR8130_assertion
a
np:Assertion
.
dgn-np:NP883704.RAKY-O0YJXRRw9C9QPJLOrh5suQvKilW7Nphe_c8vrWR8130_provenance
a
np:Provenance
.
dgn-np:NP883704.RAKY-O0YJXRRw9C9QPJLOrh5suQvKilW7Nphe_c8vrWR8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP883704.RAKY-O0YJXRRw9C9QPJLOrh5suQvKilW7Nphe_c8vrWR8130_assertion
{
miriam-gene:1666
a
ncit:C16612
.
lld:C0520679
a
ncit:C7057
.
dgn-gda:DGNafdd4b7ee01eabf4e005d186ebe2b5c4
sio:SIO_000628
miriam-gene:1666
,
lld:C0520679
;
a
sio:SIO_001121
.
}
dgn-np:NP883704.RAKY-O0YJXRRw9C9QPJLOrh5suQvKilW7Nphe_c8vrWR8130_provenance
{
dgn-np:NP883704.RAKY-O0YJXRRw9C9QPJLOrh5suQvKilW7Nphe_c8vrWR8130_assertion
dcterms:description
"[The frequencies of NADPH oxidase (NOX) polymorphisms in the p22phox subunit were similar between children with OSA and controls, except for rs6520785 and rs4673, the latter being significantly more frequent among the OSA children without deficits than with deficits (p<0.02).]. 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:21902598
;
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:NP883704.RAKY-O0YJXRRw9C9QPJLOrh5suQvKilW7Nphe_c8vrWR8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:00+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" .
}