@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y
> .
@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:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_head
{
this:
np:hasAssertion
dgn-np:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_assertion
;
np:hasProvenance
dgn-np:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_assertion
a
np:Assertion
.
dgn-np:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_provenance
a
np:Provenance
.
dgn-np:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_assertion
{
miriam-gene:1543
a
ncit:C16612
.
lld:C0152018
a
ncit:C7057
.
dgn-gda:DGNfeffd6158a6497df25ac6f3913029e6e
sio:SIO_000628
miriam-gene:1543
,
lld:C0152018
;
a
sio:SIO_001122
.
}
dgn-np:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_provenance
{
dgn-np:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_assertion
dcterms:description
"[The present results suggest that CYP1A1 3' polymorphism may be one of the promising protective factors and its wild gene type may be an indicator for higher susceptibility to esophageal cancer.]. 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:12854128
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}