@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70
> .
@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:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_head
{
this:
np:hasAssertion
dgn-np:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_assertion
;
np:hasProvenance
dgn-np:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_provenance
;
np:hasPublicationInfo
dgn-np:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_assertion
a
np:Assertion
.
dgn-np:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_provenance
a
np:Provenance
.
dgn-np:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_assertion
{
miriam-gene:4050
a
ncit:C16612
.
lld:C0520679
a
ncit:C7057
.
dgn-gda:DGN50fa4e23474128cb99567cc504e7ed86
sio:SIO_000628
miriam-gene:4050
,
lld:C0520679
;
a
sio:SIO_001121
.
}
dgn-np:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_provenance
{
dgn-np:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_assertion
dcterms:description
"[The objective of this study was to to determine the molecular mechanisms of LTB(4) pathway activation in polymorphonuclear cells (PMNs) and early vascular remodeling in OSA and the specific contribution of intermittent hypoxia (IH).]. 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:22761257
;
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:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:13+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" .
}