@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP545670.RAymK9t_AB3PfvXxU18VryFTL5e03bNkjA6J9tGJcdkl8
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP545670.RAymK9t_AB3PfvXxU18VryFTL5e03bNkjA6J9tGJcdkl8130_assertion
;
np:hasProvenance
dgn-np:NP545670.RAymK9t_AB3PfvXxU18VryFTL5e03bNkjA6J9tGJcdkl8130_provenance
;
np:hasPublicationInfo
dgn-np:NP545670.RAymK9t_AB3PfvXxU18VryFTL5e03bNkjA6J9tGJcdkl8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP545670.RAymK9t_AB3PfvXxU18VryFTL5e03bNkjA6J9tGJcdkl8130_assertion
a
np:Assertion
.
dgn-np:NP545670.RAymK9t_AB3PfvXxU18VryFTL5e03bNkjA6J9tGJcdkl8130_provenance
a
np:Provenance
.
dgn-np:NP545670.RAymK9t_AB3PfvXxU18VryFTL5e03bNkjA6J9tGJcdkl8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP545670.RAymK9t_AB3PfvXxU18VryFTL5e03bNkjA6J9tGJcdkl8130_assertion
{
miriam-gene:89832
a
ncit:C16612
.
lld:C0028043
a
ncit:C7057
.
dgn-gda:DGN1ff5a8179674db216f48ff97a05d2715
sio:SIO_000628
miriam-gene:89832
,
lld:C0028043
;
a
sio:SIO_001121
.
}
dgn-np:NP545670.RAymK9t_AB3PfvXxU18VryFTL5e03bNkjA6J9tGJcdkl8130_provenance
{
dgn-np:NP545670.RAymK9t_AB3PfvXxU18VryFTL5e03bNkjA6J9tGJcdkl8130_assertion
dcterms:description
"[We found evidence that genetic variation at CHRNA1, CHRNA2, CHRNA7, and CHRNB1 alters susceptibility to nicotine dependence, but we did not replicate any of the most significant single nucleotide polymorphism associations from the NICSNP high-density association study.]. 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:19307444
;
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:NP545670.RAymK9t_AB3PfvXxU18VryFTL5e03bNkjA6J9tGJcdkl8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:29+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" .
}