@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP50575.RAfmg2wbWoteE4VcghUAUoUAVZp1tzEMNZRf_5vvffQFk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP50575.RAfmg2wbWoteE4VcghUAUoUAVZp1tzEMNZRf_5vvffQFk130_head
{
this:
np:hasAssertion
dgn-np:NP50575.RAfmg2wbWoteE4VcghUAUoUAVZp1tzEMNZRf_5vvffQFk130_assertion
;
np:hasProvenance
dgn-np:NP50575.RAfmg2wbWoteE4VcghUAUoUAVZp1tzEMNZRf_5vvffQFk130_provenance
;
np:hasPublicationInfo
dgn-np:NP50575.RAfmg2wbWoteE4VcghUAUoUAVZp1tzEMNZRf_5vvffQFk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP50575.RAfmg2wbWoteE4VcghUAUoUAVZp1tzEMNZRf_5vvffQFk130_assertion
a
np:Assertion
.
dgn-np:NP50575.RAfmg2wbWoteE4VcghUAUoUAVZp1tzEMNZRf_5vvffQFk130_provenance
a
np:Provenance
.
dgn-np:NP50575.RAfmg2wbWoteE4VcghUAUoUAVZp1tzEMNZRf_5vvffQFk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP50575.RAfmg2wbWoteE4VcghUAUoUAVZp1tzEMNZRf_5vvffQFk130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C0152018
a
ncit:C7057
.
dgn-gda:DGN2b73d5468863ce89f01ee27d708c1054
sio:SIO_000628
miriam-gene:2952
,
lld:C0152018
;
a
sio:SIO_001122
.
}
dgn-np:NP50575.RAfmg2wbWoteE4VcghUAUoUAVZp1tzEMNZRf_5vvffQFk130_provenance
{
dgn-np:NP50575.RAfmg2wbWoteE4VcghUAUoUAVZp1tzEMNZRf_5vvffQFk130_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 ]. 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-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP50575.RAfmg2wbWoteE4VcghUAUoUAVZp1tzEMNZRf_5vvffQFk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:07+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}