@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP438103.RAm_xbfTKRq-i197wqY61KNItnHuh4-k8fSMnNvb89vr8
> .
@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:NP438103.RAm_xbfTKRq-i197wqY61KNItnHuh4-k8fSMnNvb89vr8130_head
{
this:
np:hasAssertion
dgn-np:NP438103.RAm_xbfTKRq-i197wqY61KNItnHuh4-k8fSMnNvb89vr8130_assertion
;
np:hasProvenance
dgn-np:NP438103.RAm_xbfTKRq-i197wqY61KNItnHuh4-k8fSMnNvb89vr8130_provenance
;
np:hasPublicationInfo
dgn-np:NP438103.RAm_xbfTKRq-i197wqY61KNItnHuh4-k8fSMnNvb89vr8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP438103.RAm_xbfTKRq-i197wqY61KNItnHuh4-k8fSMnNvb89vr8130_assertion
a
np:Assertion
.
dgn-np:NP438103.RAm_xbfTKRq-i197wqY61KNItnHuh4-k8fSMnNvb89vr8130_provenance
a
np:Provenance
.
dgn-np:NP438103.RAm_xbfTKRq-i197wqY61KNItnHuh4-k8fSMnNvb89vr8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP438103.RAm_xbfTKRq-i197wqY61KNItnHuh4-k8fSMnNvb89vr8130_assertion
{
miriam-gene:2070
a
ncit:C16612
.
lld:C0014859
a
ncit:C7057
.
dgn-gda:DGNa3cf766b070262fe504b43ccf80ec558
sio:SIO_000628
miriam-gene:2070
,
lld:C0014859
;
a
sio:SIO_001121
.
}
dgn-np:NP438103.RAm_xbfTKRq-i197wqY61KNItnHuh4-k8fSMnNvb89vr8130_provenance
{
dgn-np:NP438103.RAm_xbfTKRq-i197wqY61KNItnHuh4-k8fSMnNvb89vr8130_assertion
dcterms:description
"[The testing sensitivities in the predicting ESCD and ESCC in the discriminant model including EYA4 and hTERT and the five traditional risk factors (sex, age, smoking, alcohol drinking, and family history of esophageal cancer) were 70% and 80%, and testing specificities were 76% and 88% respectively.]. 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:19939248
;
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:NP438103.RAm_xbfTKRq-i197wqY61KNItnHuh4-k8fSMnNvb89vr8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:19+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" .
}