@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47262.RAj2taLFi9WTVaSrHRrWQnnpEN41m6fxfIIXV-1D4V0Jo
> .
@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 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:NP47262.RAj2taLFi9WTVaSrHRrWQnnpEN41m6fxfIIXV-1D4V0Jo130_head
{
this:
np:hasAssertion
dgn-np:NP47262.RAj2taLFi9WTVaSrHRrWQnnpEN41m6fxfIIXV-1D4V0Jo130_assertion
;
np:hasProvenance
dgn-np:NP47262.RAj2taLFi9WTVaSrHRrWQnnpEN41m6fxfIIXV-1D4V0Jo130_provenance
;
np:hasPublicationInfo
dgn-np:NP47262.RAj2taLFi9WTVaSrHRrWQnnpEN41m6fxfIIXV-1D4V0Jo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47262.RAj2taLFi9WTVaSrHRrWQnnpEN41m6fxfIIXV-1D4V0Jo130_assertion
a
np:Assertion
.
dgn-np:NP47262.RAj2taLFi9WTVaSrHRrWQnnpEN41m6fxfIIXV-1D4V0Jo130_provenance
a
np:Provenance
.
dgn-np:NP47262.RAj2taLFi9WTVaSrHRrWQnnpEN41m6fxfIIXV-1D4V0Jo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47262.RAj2taLFi9WTVaSrHRrWQnnpEN41m6fxfIIXV-1D4V0Jo130_assertion
{
miriam-gene:1234
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGNa25449704c77280556d7751aee71fd8f
sio:SIO_000628
miriam-gene:1234
,
lld:C0004096
;
a
sio:SIO_001122
.
}
dgn-np:NP47262.RAj2taLFi9WTVaSrHRrWQnnpEN41m6fxfIIXV-1D4V0Jo130_provenance
{
dgn-np:NP47262.RAj2taLFi9WTVaSrHRrWQnnpEN41m6fxfIIXV-1D4V0Jo130_assertion
dct:description
"[The chemokine receptor genes on 3p21.3 are significantly plausible candidate genes that can influence the expression of asthma. The previous association of the CCR532 deletion with protection from childhood asthma appears to be explained by linkage disequilibrium with the -G190A mutation in the CCR2 receptor gene.]. 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:20220260
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP47262.RAj2taLFi9WTVaSrHRrWQnnpEN41m6fxfIIXV-1D4V0Jo130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:21+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}