@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP182187.RAxoiqGBUI3boNflZly5cIovpdSSQbQqI7gmDlJRu15OQ
> .
@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:NP182187.RAxoiqGBUI3boNflZly5cIovpdSSQbQqI7gmDlJRu15OQ130_head
{
this:
np:hasAssertion
dgn-np:NP182187.RAxoiqGBUI3boNflZly5cIovpdSSQbQqI7gmDlJRu15OQ130_assertion
;
np:hasProvenance
dgn-np:NP182187.RAxoiqGBUI3boNflZly5cIovpdSSQbQqI7gmDlJRu15OQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP182187.RAxoiqGBUI3boNflZly5cIovpdSSQbQqI7gmDlJRu15OQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP182187.RAxoiqGBUI3boNflZly5cIovpdSSQbQqI7gmDlJRu15OQ130_assertion
a
np:Assertion
.
dgn-np:NP182187.RAxoiqGBUI3boNflZly5cIovpdSSQbQqI7gmDlJRu15OQ130_provenance
a
np:Provenance
.
dgn-np:NP182187.RAxoiqGBUI3boNflZly5cIovpdSSQbQqI7gmDlJRu15OQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP182187.RAxoiqGBUI3boNflZly5cIovpdSSQbQqI7gmDlJRu15OQ130_assertion
{
miriam-gene:1604
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGN89b40dca6cac5984941928fbd003b5ed
sio:SIO_000628
miriam-gene:1604
,
lld:C0011847
;
a
sio:SIO_001121
.
}
dgn-np:NP182187.RAxoiqGBUI3boNflZly5cIovpdSSQbQqI7gmDlJRu15OQ130_provenance
{
dgn-np:NP182187.RAxoiqGBUI3boNflZly5cIovpdSSQbQqI7gmDlJRu15OQ130_assertion
dcterms:description
"[A silent SNP in the alpha2 integrin subunit gene (echovirus 1 receptor) was frequently found in both groups, a silent heterozygotic SNP in coxsackievirus-adenovirus receptor (coxsackie B virus receptor) gene was seen in one individual in the diabetes group, whereas no variation was found in the DAF (echovirus receptor) and beta3 integrin subunit sequences (receptor for coxsackievirus A9) studied.]. 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:12629650
;
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:NP182187.RAxoiqGBUI3boNflZly5cIovpdSSQbQqI7gmDlJRu15OQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:38+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" .
}