@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4
> .
@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:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_head
{
this:
np:hasAssertion
dgn-np:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_assertion
;
np:hasProvenance
dgn-np:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_provenance
;
np:hasPublicationInfo
dgn-np:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_assertion
a
np:Assertion
.
dgn-np:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_provenance
a
np:Provenance
.
dgn-np:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_assertion
{
miriam-gene:54738
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGNf283a05f114f5a502dd9b0395ff0a4d7
sio:SIO_000628
miriam-gene:54738
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_provenance
{
dgn-np:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_assertion
dcterms:description
"[More interestingly, regression analysis of the decline of forced expiratory volume in one second (FEV(1)) by aspirin provocation revealed that 10 SNPs (P = 0.003-0.04) and four relevant haplotypes (P = 0.002-0.02) were significantly associated with the fall rate of FEV(1) by aspirin provocation, indicating that genetic polymorphisms of EMID2 could cause meaningful deficits in the upper and lower airways among AIA patients.]. 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:21086123
;
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:NP853191.RAmcXQts9kvaGtlFlW_EI6TLeMEbaEj_X2UpYSWHg5Nm4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:11+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" .
}