@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP652946.RA5kKeAwRdMyCK_30HTdLgvMG0zwlDpIKHdODdHZdrLEk
> .
@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/v3.0.0/void/
> .
dgn-np:NP652946.RA5kKeAwRdMyCK_30HTdLgvMG0zwlDpIKHdODdHZdrLEk130_head
{
this:
np:hasAssertion
dgn-np:NP652946.RA5kKeAwRdMyCK_30HTdLgvMG0zwlDpIKHdODdHZdrLEk130_assertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP652946.RA5kKeAwRdMyCK_30HTdLgvMG0zwlDpIKHdODdHZdrLEk130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP652946.RA5kKeAwRdMyCK_30HTdLgvMG0zwlDpIKHdODdHZdrLEk130_assertion
a
np:Assertion
.
dgn-np:NP652946.RA5kKeAwRdMyCK_30HTdLgvMG0zwlDpIKHdODdHZdrLEk130_provenance
a
np:Provenance
.
dgn-np:NP652946.RA5kKeAwRdMyCK_30HTdLgvMG0zwlDpIKHdODdHZdrLEk130_publicationInfo
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dgn-np:NP652946.RA5kKeAwRdMyCK_30HTdLgvMG0zwlDpIKHdODdHZdrLEk130_assertion
{
miriam-gene:5726
a
ncit:C16612
.
lld:C0010278
a
ncit:C7057
.
dgn-gda:DGNfe9787101fb87e1d6c874d74021c37b8
sio:SIO_000628
miriam-gene:5726
,
lld:C0010278
;
a
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.
}
dgn-np:NP652946.RA5kKeAwRdMyCK_30HTdLgvMG0zwlDpIKHdODdHZdrLEk130_provenance
{
dgn-np:NP652946.RA5kKeAwRdMyCK_30HTdLgvMG0zwlDpIKHdODdHZdrLEk130_assertion
dcterms:description
"[Our objective was to determine whether the nonprotective TAS2R38 polymorphisms, which render the receptor inactive, correlate with medically recalcitrant chronic rhinosinusitis (CRS) necessitating surgical intervention in the context of known risk factors, and thus identify whether the TAS2R38 genotype is an independent risk factor for patients undergoing functional endoscopic sinus surgery (FESS).]. 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:24302675
;
prov:wasDerivedFrom
dgn-void:befree-20150227
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prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP652946.RA5kKeAwRdMyCK_30HTdLgvMG0zwlDpIKHdODdHZdrLEk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:12+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
<
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> , <
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> , <
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
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"v3.0.0" .
}