@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP345882.RA4CDfS1aq58ms7oo_30zM_c7q2hY647CY-UZJLpr5sxU
> .
@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:NP345882.RA4CDfS1aq58ms7oo_30zM_c7q2hY647CY-UZJLpr5sxU130_head
{
this:
np:hasAssertion
dgn-np:NP345882.RA4CDfS1aq58ms7oo_30zM_c7q2hY647CY-UZJLpr5sxU130_assertion
;
np:hasProvenance
dgn-np:NP345882.RA4CDfS1aq58ms7oo_30zM_c7q2hY647CY-UZJLpr5sxU130_provenance
;
np:hasPublicationInfo
dgn-np:NP345882.RA4CDfS1aq58ms7oo_30zM_c7q2hY647CY-UZJLpr5sxU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP345882.RA4CDfS1aq58ms7oo_30zM_c7q2hY647CY-UZJLpr5sxU130_assertion
a
np:Assertion
.
dgn-np:NP345882.RA4CDfS1aq58ms7oo_30zM_c7q2hY647CY-UZJLpr5sxU130_provenance
a
np:Provenance
.
dgn-np:NP345882.RA4CDfS1aq58ms7oo_30zM_c7q2hY647CY-UZJLpr5sxU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP345882.RA4CDfS1aq58ms7oo_30zM_c7q2hY647CY-UZJLpr5sxU130_assertion
{
miriam-gene:2072
a
ncit:C16612
.
lld:C0546837
a
ncit:C7057
.
dgn-gda:DGNd00bf032ac45f1dc25a7debd91313dec
sio:SIO_000628
miriam-gene:2072
,
lld:C0546837
;
a
sio:SIO_001121
.
}
dgn-np:NP345882.RA4CDfS1aq58ms7oo_30zM_c7q2hY647CY-UZJLpr5sxU130_provenance
{
dgn-np:NP345882.RA4CDfS1aq58ms7oo_30zM_c7q2hY647CY-UZJLpr5sxU130_assertion
dcterms:description
"[Genetic variants in ERCC2 and ERCC4 may provide further survival prediction in addition to TNM staging system of esophageal cancer, which is more evident in the patients with early disease status.]. 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:21490450
;
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:NP345882.RA4CDfS1aq58ms7oo_30zM_c7q2hY647CY-UZJLpr5sxU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:23+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" .
}