@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP443664.RAEhDNWy5BN0dX7NRlzLt98cmMl2X4UFts6A_07twNXGM
> .
@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:NP443664.RAEhDNWy5BN0dX7NRlzLt98cmMl2X4UFts6A_07twNXGM130_assertion
;
np:hasProvenance
dgn-np:NP443664.RAEhDNWy5BN0dX7NRlzLt98cmMl2X4UFts6A_07twNXGM130_provenance
;
np:hasPublicationInfo
dgn-np:NP443664.RAEhDNWy5BN0dX7NRlzLt98cmMl2X4UFts6A_07twNXGM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP443664.RAEhDNWy5BN0dX7NRlzLt98cmMl2X4UFts6A_07twNXGM130_assertion
a
np:Assertion
.
dgn-np:NP443664.RAEhDNWy5BN0dX7NRlzLt98cmMl2X4UFts6A_07twNXGM130_provenance
a
np:Provenance
.
dgn-np:NP443664.RAEhDNWy5BN0dX7NRlzLt98cmMl2X4UFts6A_07twNXGM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP443664.RAEhDNWy5BN0dX7NRlzLt98cmMl2X4UFts6A_07twNXGM130_assertion
{
miriam-gene:7367
a
ncit:C16612
.
lld:C0152013
a
ncit:C7057
.
dgn-gda:DGN0878cba6d39d7c93d079f3eb40a8f2e8
sio:SIO_000628
miriam-gene:7367
,
lld:C0152013
;
a
sio:SIO_001121
.
}
dgn-np:NP443664.RAEhDNWy5BN0dX7NRlzLt98cmMl2X4UFts6A_07twNXGM130_provenance
{
dgn-np:NP443664.RAEhDNWy5BN0dX7NRlzLt98cmMl2X4UFts6A_07twNXGM130_assertion
dcterms:description
"[The association of the UGT2B17 deletion with increased lung adenocarcinoma in women is consistent with its association with decreased NNAL glucuronidation rates in women and with studies showing that NNAL is a selective inducer of lung adenocarcinoma in experimental animals.]. 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:17416778
;
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:NP443664.RAEhDNWy5BN0dX7NRlzLt98cmMl2X4UFts6A_07twNXGM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:24+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" .
}