@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP106770.RAL-PheFwFMN54EC21I-0st3g9AjgHOUBcKqpcve7F38o
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP106770.RAL-PheFwFMN54EC21I-0st3g9AjgHOUBcKqpcve7F38o130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP106770.RAL-PheFwFMN54EC21I-0st3g9AjgHOUBcKqpcve7F38o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP106770.RAL-PheFwFMN54EC21I-0st3g9AjgHOUBcKqpcve7F38o130_assertion
a
np:Assertion
.
dgn-np:NP106770.RAL-PheFwFMN54EC21I-0st3g9AjgHOUBcKqpcve7F38o130_provenance
a
np:Provenance
.
dgn-np:NP106770.RAL-PheFwFMN54EC21I-0st3g9AjgHOUBcKqpcve7F38o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP106770.RAL-PheFwFMN54EC21I-0st3g9AjgHOUBcKqpcve7F38o130_assertion
{
miriam-gene:217
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGN6a86daf539eafcaf2ecef62e10f2784b
sio:SIO_000628
miriam-gene:217
,
lld:C0007137
;
a
sio:SIO_001122
.
}
dgn-np:NP106770.RAL-PheFwFMN54EC21I-0st3g9AjgHOUBcKqpcve7F38o130_provenance
{
dgn-np:NP106770.RAL-PheFwFMN54EC21I-0st3g9AjgHOUBcKqpcve7F38o130_assertion
dcterms:description
"[The genetic variations of ADH1B His47Arg and ALDH2 Glu487Lys are susceptible loci for ESCC in Chinese Han population and interact substantially with alcohol consumption. The individuals carrying both risky genotypes have a higher baseline risk of ESCC.]. 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:21157980
;
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 .
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dgn-np:NP106770.RAL-PheFwFMN54EC21I-0st3g9AjgHOUBcKqpcve7F38o130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:39+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
<
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> , <
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> , <
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
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pav:version
"v3.0.0" .
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