@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP373285.RA46ZB9UQ3oAxevpFM19C6czNmTisSF6dYnFwvRJVS4JQ
> .
@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:NP373285.RA46ZB9UQ3oAxevpFM19C6czNmTisSF6dYnFwvRJVS4JQ130_head
{
this:
np:hasAssertion
dgn-np:NP373285.RA46ZB9UQ3oAxevpFM19C6czNmTisSF6dYnFwvRJVS4JQ130_assertion
;
np:hasProvenance
dgn-np:NP373285.RA46ZB9UQ3oAxevpFM19C6czNmTisSF6dYnFwvRJVS4JQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP373285.RA46ZB9UQ3oAxevpFM19C6czNmTisSF6dYnFwvRJVS4JQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP373285.RA46ZB9UQ3oAxevpFM19C6czNmTisSF6dYnFwvRJVS4JQ130_assertion
a
np:Assertion
.
dgn-np:NP373285.RA46ZB9UQ3oAxevpFM19C6czNmTisSF6dYnFwvRJVS4JQ130_provenance
a
np:Provenance
.
dgn-np:NP373285.RA46ZB9UQ3oAxevpFM19C6czNmTisSF6dYnFwvRJVS4JQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP373285.RA46ZB9UQ3oAxevpFM19C6czNmTisSF6dYnFwvRJVS4JQ130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0520679
a
ncit:C7057
.
dgn-gda:DGNc127dc9113cf902cbe00feaf3f0f9acf
sio:SIO_000628
miriam-gene:348
,
lld:C0520679
;
a
sio:SIO_001121
.
}
dgn-np:NP373285.RA46ZB9UQ3oAxevpFM19C6czNmTisSF6dYnFwvRJVS4JQ130_provenance
{
dgn-np:NP373285.RA46ZB9UQ3oAxevpFM19C6czNmTisSF6dYnFwvRJVS4JQ130_assertion
dcterms:description
"[The APOE polymorphisms may modulate the effects of intermittent hypoxia and sleep fragmentation in the sleep architecture of OSAS patients, and that the presence of the ε2 allele may serve as a biological marker for the identification of a subgroup of patients who are more likely to suffer with OSAS detrimental effects on sleep, impacting not only the daily functioning, but also their quality of life.]. 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:21864519
;
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:NP373285.RA46ZB9UQ3oAxevpFM19C6czNmTisSF6dYnFwvRJVS4JQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:38+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" .
}