@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec
> .
@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:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_head
{
this:
np:hasAssertion
dgn-np:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_assertion
;
np:hasProvenance
dgn-np:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_provenance
;
np:hasPublicationInfo
dgn-np:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_assertion
a
np:Assertion
.
dgn-np:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_provenance
a
np:Provenance
.
dgn-np:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_assertion
{
miriam-gene:7507
a
ncit:C16612
.
lld:C1559154
a
ncit:C7057
.
dgn-gda:DGN988cc30e4e19421a41674cffa8c42724
sio:SIO_000628
miriam-gene:7507
,
lld:C1559154
;
a
sio:SIO_001121
.
}
dgn-np:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_provenance
{
dgn-np:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_assertion
dcterms:description
"[The hereditary genetic variants in XPA and XPC can serve as independent predictors of the clinical outcome of patients with ESCC, especially in those who are treated with esophagectomy and undergo chemoradiation.]. 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:22941172
;
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:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:50+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" .
}