@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP970467.RAvD-_WU08LuAYIUHLytexXK4Ih3i3-drGOJ2Hi3DOHVc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP970467.RAvD-_WU08LuAYIUHLytexXK4Ih3i3-drGOJ2Hi3DOHVc130_head
{
this:
np:hasAssertion
dgn-np:NP970467.RAvD-_WU08LuAYIUHLytexXK4Ih3i3-drGOJ2Hi3DOHVc130_assertion
;
np:hasProvenance
dgn-np:NP970467.RAvD-_WU08LuAYIUHLytexXK4Ih3i3-drGOJ2Hi3DOHVc130_provenance
;
np:hasPublicationInfo
dgn-np:NP970467.RAvD-_WU08LuAYIUHLytexXK4Ih3i3-drGOJ2Hi3DOHVc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP970467.RAvD-_WU08LuAYIUHLytexXK4Ih3i3-drGOJ2Hi3DOHVc130_assertion
a
np:Assertion
.
dgn-np:NP970467.RAvD-_WU08LuAYIUHLytexXK4Ih3i3-drGOJ2Hi3DOHVc130_provenance
a
np:Provenance
.
dgn-np:NP970467.RAvD-_WU08LuAYIUHLytexXK4Ih3i3-drGOJ2Hi3DOHVc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP970467.RAvD-_WU08LuAYIUHLytexXK4Ih3i3-drGOJ2Hi3DOHVc130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0279628
a
ncit:C7057
.
dgn-gda:DGN574b80ae7381eccf2991cbe94f8f2da6
sio:SIO_000628
miriam-gene:1029
,
lld:C0279628
;
a
sio:SIO_001121
.
}
dgn-np:NP970467.RAvD-_WU08LuAYIUHLytexXK4Ih3i3-drGOJ2Hi3DOHVc130_provenance
{
dgn-np:NP970467.RAvD-_WU08LuAYIUHLytexXK4Ih3i3-drGOJ2Hi3DOHVc130_assertion
dcterms:description
"[The ESCC and EAC genomes showed some copy number abnormalities with similar frequencies (eg, CDKN2A, EGFR, KRAS, MYC, CDK6, MET) but also many copy number abnormalities with different frequencies between histologic types, most of which were amplification events.]. 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:22450065
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP970467.RAvD-_WU08LuAYIUHLytexXK4Ih3i3-drGOJ2Hi3DOHVc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:04+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}