@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP632021.RAp8uWRzm-sT8fSEti8cy1YZYFwGVmzBLKPocjZi53ung
> .
@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:NP632021.RAp8uWRzm-sT8fSEti8cy1YZYFwGVmzBLKPocjZi53ung130_head
{
this:
np:hasAssertion
dgn-np:NP632021.RAp8uWRzm-sT8fSEti8cy1YZYFwGVmzBLKPocjZi53ung130_assertion
;
np:hasProvenance
dgn-np:NP632021.RAp8uWRzm-sT8fSEti8cy1YZYFwGVmzBLKPocjZi53ung130_provenance
;
np:hasPublicationInfo
dgn-np:NP632021.RAp8uWRzm-sT8fSEti8cy1YZYFwGVmzBLKPocjZi53ung130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP632021.RAp8uWRzm-sT8fSEti8cy1YZYFwGVmzBLKPocjZi53ung130_assertion
a
np:Assertion
.
dgn-np:NP632021.RAp8uWRzm-sT8fSEti8cy1YZYFwGVmzBLKPocjZi53ung130_provenance
a
np:Provenance
.
dgn-np:NP632021.RAp8uWRzm-sT8fSEti8cy1YZYFwGVmzBLKPocjZi53ung130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP632021.RAp8uWRzm-sT8fSEti8cy1YZYFwGVmzBLKPocjZi53ung130_assertion
{
miriam-gene:7442
a
ncit:C16612
.
lld:C0010201
a
ncit:C7057
.
dgn-gda:DGNff09e9c44685ae6e051e42965cf630db
sio:SIO_000628
miriam-gene:7442
,
lld:C0010201
;
a
sio:SIO_001121
.
}
dgn-np:NP632021.RAp8uWRzm-sT8fSEti8cy1YZYFwGVmzBLKPocjZi53ung130_provenance
{
dgn-np:NP632021.RAp8uWRzm-sT8fSEti8cy1YZYFwGVmzBLKPocjZi53ung130_assertion
dcterms:description
"[TRPV1 expression and activity appear to be altered under pathophysiological conditions such as chronic cough and airway hypersensitivity, whereas TRPV4 single nucleotide polymorphisms (SNP) are associated with chronic obstructive pulmonary disease.]. 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:20639579
;
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:NP632021.RAp8uWRzm-sT8fSEti8cy1YZYFwGVmzBLKPocjZi53ung130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:21+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" .
}