@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP690882.RA45jMmhcpSGGJmdah9ZSSIgSOPWh12huU2ZO7nMXEsKg
> .
@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:NP690882.RA45jMmhcpSGGJmdah9ZSSIgSOPWh12huU2ZO7nMXEsKg130_head
{
this:
np:hasAssertion
dgn-np:NP690882.RA45jMmhcpSGGJmdah9ZSSIgSOPWh12huU2ZO7nMXEsKg130_assertion
;
np:hasProvenance
dgn-np:NP690882.RA45jMmhcpSGGJmdah9ZSSIgSOPWh12huU2ZO7nMXEsKg130_provenance
;
np:hasPublicationInfo
dgn-np:NP690882.RA45jMmhcpSGGJmdah9ZSSIgSOPWh12huU2ZO7nMXEsKg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP690882.RA45jMmhcpSGGJmdah9ZSSIgSOPWh12huU2ZO7nMXEsKg130_assertion
a
np:Assertion
.
dgn-np:NP690882.RA45jMmhcpSGGJmdah9ZSSIgSOPWh12huU2ZO7nMXEsKg130_provenance
a
np:Provenance
.
dgn-np:NP690882.RA45jMmhcpSGGJmdah9ZSSIgSOPWh12huU2ZO7nMXEsKg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP690882.RA45jMmhcpSGGJmdah9ZSSIgSOPWh12huU2ZO7nMXEsKg130_assertion
{
miriam-gene:1141
a
ncit:C16612
.
lld:C0012833
a
ncit:C7057
.
dgn-gda:DGN4e35f6c1ba58db587cc7fda8a5c00379
sio:SIO_000628
miriam-gene:1141
,
lld:C0012833
;
a
sio:SIO_001121
.
}
dgn-np:NP690882.RA45jMmhcpSGGJmdah9ZSSIgSOPWh12huU2ZO7nMXEsKg130_provenance
{
dgn-np:NP690882.RA45jMmhcpSGGJmdah9ZSSIgSOPWh12huU2ZO7nMXEsKg130_assertion
dcterms:description
"[Individuals with the minor allele of CHRNB2 variants experienced less nausea than did those without the minor allele, consistent with previously reported findings for CHRNB2 and the occurrence of nausea and dizziness as a consequence of first smoking attempt in adolescents, and with the known neurophysiology of nausea.]. 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:21606948
;
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:NP690882.RA45jMmhcpSGGJmdah9ZSSIgSOPWh12huU2ZO7nMXEsKg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:00+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" .
}