@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47276.RAfbqMyrbroGFGRnInL3_pM46zyHbqrWL9-jvEE0e_WG0
> .
@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:NP47276.RAfbqMyrbroGFGRnInL3_pM46zyHbqrWL9-jvEE0e_WG0130_head
{
this:
np:hasAssertion
dgn-np:NP47276.RAfbqMyrbroGFGRnInL3_pM46zyHbqrWL9-jvEE0e_WG0130_assertion
;
np:hasProvenance
dgn-np:NP47276.RAfbqMyrbroGFGRnInL3_pM46zyHbqrWL9-jvEE0e_WG0130_provenance
;
np:hasPublicationInfo
dgn-np:NP47276.RAfbqMyrbroGFGRnInL3_pM46zyHbqrWL9-jvEE0e_WG0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47276.RAfbqMyrbroGFGRnInL3_pM46zyHbqrWL9-jvEE0e_WG0130_assertion
a
np:Assertion
.
dgn-np:NP47276.RAfbqMyrbroGFGRnInL3_pM46zyHbqrWL9-jvEE0e_WG0130_provenance
a
np:Provenance
.
dgn-np:NP47276.RAfbqMyrbroGFGRnInL3_pM46zyHbqrWL9-jvEE0e_WG0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47276.RAfbqMyrbroGFGRnInL3_pM46zyHbqrWL9-jvEE0e_WG0130_assertion
{
miriam-gene:1232
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGNd08081c54a6f783b6f0483b7d5629e82
sio:SIO_000628
miriam-gene:1232
,
lld:C0004096
;
a
sio:SIO_001122
.
}
dgn-np:NP47276.RAfbqMyrbroGFGRnInL3_pM46zyHbqrWL9-jvEE0e_WG0130_provenance
{
dgn-np:NP47276.RAfbqMyrbroGFGRnInL3_pM46zyHbqrWL9-jvEE0e_WG0130_assertion
dcterms: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:NP47276.RAfbqMyrbroGFGRnInL3_pM46zyHbqrWL9-jvEE0e_WG0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}