@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP490301.RADF0Tp8VHudYHmP2_rn1WfPs3WE_1swgr5ub9VBfcpAE
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP490301.RADF0Tp8VHudYHmP2_rn1WfPs3WE_1swgr5ub9VBfcpAE130_head
{
this:
np:hasAssertion
dgn-np:NP490301.RADF0Tp8VHudYHmP2_rn1WfPs3WE_1swgr5ub9VBfcpAE130_assertion
;
np:hasProvenance
dgn-np:NP490301.RADF0Tp8VHudYHmP2_rn1WfPs3WE_1swgr5ub9VBfcpAE130_provenance
;
np:hasPublicationInfo
dgn-np:NP490301.RADF0Tp8VHudYHmP2_rn1WfPs3WE_1swgr5ub9VBfcpAE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP490301.RADF0Tp8VHudYHmP2_rn1WfPs3WE_1swgr5ub9VBfcpAE130_assertion
a
np:Assertion
.
dgn-np:NP490301.RADF0Tp8VHudYHmP2_rn1WfPs3WE_1swgr5ub9VBfcpAE130_provenance
a
np:Provenance
.
dgn-np:NP490301.RADF0Tp8VHudYHmP2_rn1WfPs3WE_1swgr5ub9VBfcpAE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP490301.RADF0Tp8VHudYHmP2_rn1WfPs3WE_1swgr5ub9VBfcpAE130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGNae12dd329cc39785279ef29080ad84ff
sio:SIO_000628
miriam-gene:3630
,
lld:C0011847
;
a
sio:SIO_001121
.
}
dgn-np:NP490301.RADF0Tp8VHudYHmP2_rn1WfPs3WE_1swgr5ub9VBfcpAE130_provenance
{
dgn-np:NP490301.RADF0Tp8VHudYHmP2_rn1WfPs3WE_1swgr5ub9VBfcpAE130_assertion
dcterms:description
"[We examined whether variation in the gene for E-selectin (SELE), a biomarker of endothelial dysfunction, was associated with levels of E-selectin or diabetes quantitative traits (including fasting levels of insulin and hemoglobin A(1c)) in 719 nondiabetic participants of the Nurses' Health Study or with risk of diabetes in 602 incident (over 10 years of follow-up) cases and 655 control women matched for age, race, and fasting status.]. 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:15833936
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP490301.RADF0Tp8VHudYHmP2_rn1WfPs3WE_1swgr5ub9VBfcpAE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:27+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}