@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP749501.RA1um9S6B0IEG4as9pqfcsdrYawLdChHQDq3Arz1MvXHA
> .
@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:NP749501.RA1um9S6B0IEG4as9pqfcsdrYawLdChHQDq3Arz1MvXHA130_head
{
this:
np:hasAssertion
dgn-np:NP749501.RA1um9S6B0IEG4as9pqfcsdrYawLdChHQDq3Arz1MvXHA130_assertion
;
np:hasProvenance
dgn-np:NP749501.RA1um9S6B0IEG4as9pqfcsdrYawLdChHQDq3Arz1MvXHA130_provenance
;
np:hasPublicationInfo
dgn-np:NP749501.RA1um9S6B0IEG4as9pqfcsdrYawLdChHQDq3Arz1MvXHA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP749501.RA1um9S6B0IEG4as9pqfcsdrYawLdChHQDq3Arz1MvXHA130_assertion
a
np:Assertion
.
dgn-np:NP749501.RA1um9S6B0IEG4as9pqfcsdrYawLdChHQDq3Arz1MvXHA130_provenance
a
np:Provenance
.
dgn-np:NP749501.RA1um9S6B0IEG4as9pqfcsdrYawLdChHQDq3Arz1MvXHA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP749501.RA1um9S6B0IEG4as9pqfcsdrYawLdChHQDq3Arz1MvXHA130_assertion
{
miriam-gene:4193
a
ncit:C16612
.
lld:C0014859
a
ncit:C7057
.
dgn-gda:DGN97233b56ede734fd330a7de615290c0f
sio:SIO_000628
miriam-gene:4193
,
lld:C0014859
;
a
sio:SIO_001121
.
}
dgn-np:NP749501.RA1um9S6B0IEG4as9pqfcsdrYawLdChHQDq3Arz1MvXHA130_provenance
{
dgn-np:NP749501.RA1um9S6B0IEG4as9pqfcsdrYawLdChHQDq3Arz1MvXHA130_assertion
dcterms:description
"[These results suggest that the 11q13 amplicon and MDM2 may play an important role in the progression of esophageal cancer, and an accumulation of genomic abnormalities may result in poor prognosis.]. 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:9296509
;
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:NP749501.RA1um9S6B0IEG4as9pqfcsdrYawLdChHQDq3Arz1MvXHA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:34+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" .
}