@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP770176.RAi2-rhTQVyK5twds_lOwjv6TJQlzaQN4a7Wr2K55xEWM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP770176.RAi2-rhTQVyK5twds_lOwjv6TJQlzaQN4a7Wr2K55xEWM130_head
{
this:
np:hasAssertion
dgn-np:NP770176.RAi2-rhTQVyK5twds_lOwjv6TJQlzaQN4a7Wr2K55xEWM130_assertion
;
np:hasProvenance
dgn-np:NP770176.RAi2-rhTQVyK5twds_lOwjv6TJQlzaQN4a7Wr2K55xEWM130_provenance
;
np:hasPublicationInfo
dgn-np:NP770176.RAi2-rhTQVyK5twds_lOwjv6TJQlzaQN4a7Wr2K55xEWM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP770176.RAi2-rhTQVyK5twds_lOwjv6TJQlzaQN4a7Wr2K55xEWM130_assertion
a
np:Assertion
.
dgn-np:NP770176.RAi2-rhTQVyK5twds_lOwjv6TJQlzaQN4a7Wr2K55xEWM130_provenance
a
np:Provenance
.
dgn-np:NP770176.RAi2-rhTQVyK5twds_lOwjv6TJQlzaQN4a7Wr2K55xEWM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP770176.RAi2-rhTQVyK5twds_lOwjv6TJQlzaQN4a7Wr2K55xEWM130_assertion
{
miriam-gene:57105
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN9e41c94fbd24ccc6d82a8b5eb637892a
sio:SIO_000628
miriam-gene:57105
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP770176.RAi2-rhTQVyK5twds_lOwjv6TJQlzaQN4a7Wr2K55xEWM130_provenance
{
dgn-np:NP770176.RAi2-rhTQVyK5twds_lOwjv6TJQlzaQN4a7Wr2K55xEWM130_assertion
dcterms:description
"[The sequence variants of CysLTR2 may affect its transcription and the stability of its mRNA, resulting in altered expression of CysLTR2 protein, which in turn causes some asthmatics to be susceptible to aspirin hypersensitivity.]. 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:19840403
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP770176.RAi2-rhTQVyK5twds_lOwjv6TJQlzaQN4a7Wr2K55xEWM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:34+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}