@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP597297.RA9FLxBIRyMWBuD5XGEZxodbMtWZfetU38MTlpYGIpH2M
> .
@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:NP597297.RA9FLxBIRyMWBuD5XGEZxodbMtWZfetU38MTlpYGIpH2M130_assertion
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np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP597297.RA9FLxBIRyMWBuD5XGEZxodbMtWZfetU38MTlpYGIpH2M130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP597297.RA9FLxBIRyMWBuD5XGEZxodbMtWZfetU38MTlpYGIpH2M130_assertion
a
np:Assertion
.
dgn-np:NP597297.RA9FLxBIRyMWBuD5XGEZxodbMtWZfetU38MTlpYGIpH2M130_provenance
a
np:Provenance
.
dgn-np:NP597297.RA9FLxBIRyMWBuD5XGEZxodbMtWZfetU38MTlpYGIpH2M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP597297.RA9FLxBIRyMWBuD5XGEZxodbMtWZfetU38MTlpYGIpH2M130_assertion
{
miriam-gene:2068
a
ncit:C16612
.
lld:C0279626
a
ncit:C7057
.
dgn-gda:DGN9f698a62f186830b4f8b671ceaf98b67
sio:SIO_000628
miriam-gene:2068
,
lld:C0279626
;
a
sio:SIO_001121
.
}
dgn-np:NP597297.RA9FLxBIRyMWBuD5XGEZxodbMtWZfetU38MTlpYGIpH2M130_provenance
{
dgn-np:NP597297.RA9FLxBIRyMWBuD5XGEZxodbMtWZfetU38MTlpYGIpH2M130_assertion
dcterms:description
"[Using the median of relative expression level in controls as the cutoff point, results also demonstrated an increased risk for ESCC associated with reduced expression of hMSH2, XRCC, XPD, and MGMT.]. 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:17479411
;
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 .
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dgn-np:NP597297.RA9FLxBIRyMWBuD5XGEZxodbMtWZfetU38MTlpYGIpH2M130_publicationInfo
{
this:
dcterms:created
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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
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pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
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"v2.1.0" .
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