@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP42736.RA2Th7XV2qcfcPO2vx09C4OFd0CILQ-uyKnryBly73Tls
> .
@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:NP42736.RA2Th7XV2qcfcPO2vx09C4OFd0CILQ-uyKnryBly73Tls130_head
{
this:
np:hasAssertion
dgn-np:NP42736.RA2Th7XV2qcfcPO2vx09C4OFd0CILQ-uyKnryBly73Tls130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP42736.RA2Th7XV2qcfcPO2vx09C4OFd0CILQ-uyKnryBly73Tls130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP42736.RA2Th7XV2qcfcPO2vx09C4OFd0CILQ-uyKnryBly73Tls130_assertion
a
np:Assertion
.
dgn-np:NP42736.RA2Th7XV2qcfcPO2vx09C4OFd0CILQ-uyKnryBly73Tls130_provenance
a
np:Provenance
.
dgn-np:NP42736.RA2Th7XV2qcfcPO2vx09C4OFd0CILQ-uyKnryBly73Tls130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP42736.RA2Th7XV2qcfcPO2vx09C4OFd0CILQ-uyKnryBly73Tls130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C0546837
a
ncit:C7057
.
dgn-gda:DGNf89e25f1fd8a183b230d11842f8d5906
sio:SIO_000628
miriam-gene:2952
,
lld:C0546837
;
a
sio:SIO_001122
.
}
dgn-np:NP42736.RA2Th7XV2qcfcPO2vx09C4OFd0CILQ-uyKnryBly73Tls130_provenance
{
dgn-np:NP42736.RA2Th7XV2qcfcPO2vx09C4OFd0CILQ-uyKnryBly73Tls130_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. mEH slow allele variant, associated with the progression of esophageal precancerous lesions, may contribute to the high susceptibility to esophageal carcinoma.]. 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:NP42736.RA2Th7XV2qcfcPO2vx09C4OFd0CILQ-uyKnryBly73Tls130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:19+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
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prv:usedData
dgn-void:disgenetrdf
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pav:authoredBy
<
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> , <
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> , <
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
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