@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP643972.RA6bbJ3jDOi2tJEKIrUdSlv6qhNKWVQtBgIET_8cWJ69U
> .
@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:NP643972.RA6bbJ3jDOi2tJEKIrUdSlv6qhNKWVQtBgIET_8cWJ69U130_head
{
this:
np:hasAssertion
dgn-np:NP643972.RA6bbJ3jDOi2tJEKIrUdSlv6qhNKWVQtBgIET_8cWJ69U130_assertion
;
np:hasProvenance
dgn-np:NP643972.RA6bbJ3jDOi2tJEKIrUdSlv6qhNKWVQtBgIET_8cWJ69U130_provenance
;
np:hasPublicationInfo
dgn-np:NP643972.RA6bbJ3jDOi2tJEKIrUdSlv6qhNKWVQtBgIET_8cWJ69U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP643972.RA6bbJ3jDOi2tJEKIrUdSlv6qhNKWVQtBgIET_8cWJ69U130_assertion
a
np:Assertion
.
dgn-np:NP643972.RA6bbJ3jDOi2tJEKIrUdSlv6qhNKWVQtBgIET_8cWJ69U130_provenance
a
np:Provenance
.
dgn-np:NP643972.RA6bbJ3jDOi2tJEKIrUdSlv6qhNKWVQtBgIET_8cWJ69U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP643972.RA6bbJ3jDOi2tJEKIrUdSlv6qhNKWVQtBgIET_8cWJ69U130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0520679
a
ncit:C7057
.
dgn-gda:DGN9c18938597be3fd81502ce6096dce28e
sio:SIO_000628
miriam-gene:3630
,
lld:C0520679
;
a
sio:SIO_001121
.
}
dgn-np:NP643972.RA6bbJ3jDOi2tJEKIrUdSlv6qhNKWVQtBgIET_8cWJ69U130_provenance
{
dgn-np:NP643972.RA6bbJ3jDOi2tJEKIrUdSlv6qhNKWVQtBgIET_8cWJ69U130_assertion
dcterms:description
"[Childhood OSA is associated with higher plasma MIF, hsCRP, and fasting insulin levels that promote cardiometabolic risk, and the MIF gene SNP rs10433310 may account for some of the variance in such risk.]. 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:22451332
;
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:NP643972.RA6bbJ3jDOi2tJEKIrUdSlv6qhNKWVQtBgIET_8cWJ69U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:28+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" .
}