@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP864904.RAH5SgALeKDB5Jyq9n5zwMIt7Bu8kl_4aZCgHiPFQeebo
> .
@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:NP864904.RAH5SgALeKDB5Jyq9n5zwMIt7Bu8kl_4aZCgHiPFQeebo130_head
{
this:
np:hasAssertion
dgn-np:NP864904.RAH5SgALeKDB5Jyq9n5zwMIt7Bu8kl_4aZCgHiPFQeebo130_assertion
;
np:hasProvenance
dgn-np:NP864904.RAH5SgALeKDB5Jyq9n5zwMIt7Bu8kl_4aZCgHiPFQeebo130_provenance
;
np:hasPublicationInfo
dgn-np:NP864904.RAH5SgALeKDB5Jyq9n5zwMIt7Bu8kl_4aZCgHiPFQeebo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP864904.RAH5SgALeKDB5Jyq9n5zwMIt7Bu8kl_4aZCgHiPFQeebo130_assertion
a
np:Assertion
.
dgn-np:NP864904.RAH5SgALeKDB5Jyq9n5zwMIt7Bu8kl_4aZCgHiPFQeebo130_provenance
a
np:Provenance
.
dgn-np:NP864904.RAH5SgALeKDB5Jyq9n5zwMIt7Bu8kl_4aZCgHiPFQeebo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP864904.RAH5SgALeKDB5Jyq9n5zwMIt7Bu8kl_4aZCgHiPFQeebo130_assertion
{
miriam-gene:4255
a
ncit:C16612
.
lld:C0279626
a
ncit:C7057
.
dgn-gda:DGN111f9905debd2bff0303e6f302f1272f
sio:SIO_000628
miriam-gene:4255
,
lld:C0279626
;
a
sio:SIO_001121
.
}
dgn-np:NP864904.RAH5SgALeKDB5Jyq9n5zwMIt7Bu8kl_4aZCgHiPFQeebo130_provenance
{
dgn-np:NP864904.RAH5SgALeKDB5Jyq9n5zwMIt7Bu8kl_4aZCgHiPFQeebo130_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 .
}
dgn-np:NP864904.RAH5SgALeKDB5Jyq9n5zwMIt7Bu8kl_4aZCgHiPFQeebo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:48+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" .
}