@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP454425.RA8yU6Fh0hUU6aXWY_bokvTNmVq9rqicCYJvNyFS4X_4c
> .
@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:NP454425.RA8yU6Fh0hUU6aXWY_bokvTNmVq9rqicCYJvNyFS4X_4c130_head
{
this:
np:hasAssertion
dgn-np:NP454425.RA8yU6Fh0hUU6aXWY_bokvTNmVq9rqicCYJvNyFS4X_4c130_assertion
;
np:hasProvenance
dgn-np:NP454425.RA8yU6Fh0hUU6aXWY_bokvTNmVq9rqicCYJvNyFS4X_4c130_provenance
;
np:hasPublicationInfo
dgn-np:NP454425.RA8yU6Fh0hUU6aXWY_bokvTNmVq9rqicCYJvNyFS4X_4c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP454425.RA8yU6Fh0hUU6aXWY_bokvTNmVq9rqicCYJvNyFS4X_4c130_assertion
a
np:Assertion
.
dgn-np:NP454425.RA8yU6Fh0hUU6aXWY_bokvTNmVq9rqicCYJvNyFS4X_4c130_provenance
a
np:Provenance
.
dgn-np:NP454425.RA8yU6Fh0hUU6aXWY_bokvTNmVq9rqicCYJvNyFS4X_4c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP454425.RA8yU6Fh0hUU6aXWY_bokvTNmVq9rqicCYJvNyFS4X_4c130_assertion
{
miriam-gene:11251
a
ncit:C16612
.
lld:C0263338
a
ncit:C7057
.
dgn-gda:DGN92c76d7a56a689480f8ac5f51f42405b
sio:SIO_000628
miriam-gene:11251
,
lld:C0263338
;
a
sio:SIO_001121
.
}
dgn-np:NP454425.RA8yU6Fh0hUU6aXWY_bokvTNmVq9rqicCYJvNyFS4X_4c130_provenance
{
dgn-np:NP454425.RA8yU6Fh0hUU6aXWY_bokvTNmVq9rqicCYJvNyFS4X_4c130_assertion
dcterms:description
"[No significant differences were detected in the genotype and allele frequencies of the two CRTH2 polymorphisms between the CU and NC groups, and no significant associations were observed with clinical parameters, such as atopy status, serum total IgE, prevalence of autoantibodies and duration of CU.]. 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:19290788
;
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:NP454425.RA8yU6Fh0hUU6aXWY_bokvTNmVq9rqicCYJvNyFS4X_4c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:31+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" .
}