@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U
> .
@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:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_head
{
this:
np:hasAssertion
dgn-np:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_assertion
;
np:hasProvenance
dgn-np:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_provenance
;
np:hasPublicationInfo
dgn-np:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_assertion
a
np:Assertion
.
dgn-np:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_provenance
a
np:Provenance
.
dgn-np:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_assertion
{
miriam-gene:3240
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN78c0dcd5ca50dc7eb9be50235bdd73ab
sio:SIO_000628
miriam-gene:3240
,
lld:C0007222
;
a
sio:SIO_001122
.
}
dgn-np:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_provenance
{
dgn-np:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_assertion
dcterms:description
"[These results suggest that haptoglobin phenotype is an important risk factor in determining susceptibility to cardiovascular disease in obstructive sleep apnea syndrome, which may be mediated by the decreased antioxidant and antiinflammatory actions of the haptoglobin 2 allelic protein product.]. 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:12938813
;
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:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:27+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" .
}