@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus
> .
@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:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_head
{
this:
np:hasAssertion
dgn-np:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_assertion
;
np:hasProvenance
dgn-np:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_provenance
;
np:hasPublicationInfo
dgn-np:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_assertion
a
np:Assertion
.
dgn-np:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_provenance
a
np:Provenance
.
dgn-np:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_assertion
{
miriam-gene:929
a
ncit:C16612
.
lld:C0477474
a
ncit:C7057
.
dgn-gda:DGN21e84266892dd577335746bd32008e48
sio:SIO_000628
miriam-gene:929
,
lld:C0477474
;
a
sio:SIO_001122
.
}
dgn-np:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_provenance
{
dgn-np:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_assertion
dct:description
"[ Our results contradict previous reports that have found a protective effect of the T allele of SNP rs2569190 (C-159T) against atopic disorders. Nevertheless, these results confirm the importance of polymorphisms in CD14 in the development of atopy, and future studies of this gene region will need to account for linkage disequilibrium and environmental exposures unique to the study population.]. 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:15867866
;
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:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_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" .
}