@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP483477.RAzOeixTAlwEWmZmSxiFSjAyhVHRKPYzt6tBw_XvCOMX4
> .
@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:NP483477.RAzOeixTAlwEWmZmSxiFSjAyhVHRKPYzt6tBw_XvCOMX4130_head
{
this:
np:hasAssertion
dgn-np:NP483477.RAzOeixTAlwEWmZmSxiFSjAyhVHRKPYzt6tBw_XvCOMX4130_assertion
;
np:hasProvenance
dgn-np:NP483477.RAzOeixTAlwEWmZmSxiFSjAyhVHRKPYzt6tBw_XvCOMX4130_provenance
;
np:hasPublicationInfo
dgn-np:NP483477.RAzOeixTAlwEWmZmSxiFSjAyhVHRKPYzt6tBw_XvCOMX4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP483477.RAzOeixTAlwEWmZmSxiFSjAyhVHRKPYzt6tBw_XvCOMX4130_assertion
a
np:Assertion
.
dgn-np:NP483477.RAzOeixTAlwEWmZmSxiFSjAyhVHRKPYzt6tBw_XvCOMX4130_provenance
a
np:Provenance
.
dgn-np:NP483477.RAzOeixTAlwEWmZmSxiFSjAyhVHRKPYzt6tBw_XvCOMX4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP483477.RAzOeixTAlwEWmZmSxiFSjAyhVHRKPYzt6tBw_XvCOMX4130_assertion
{
miriam-gene:4233
a
ncit:C16612
.
lld:C0279626
a
ncit:C7057
.
dgn-gda:DGN136643aeb4440b23d398d8d337dc8d17
sio:SIO_000628
miriam-gene:4233
,
lld:C0279626
;
a
sio:SIO_001121
.
}
dgn-np:NP483477.RAzOeixTAlwEWmZmSxiFSjAyhVHRKPYzt6tBw_XvCOMX4130_provenance
{
dgn-np:NP483477.RAzOeixTAlwEWmZmSxiFSjAyhVHRKPYzt6tBw_XvCOMX4130_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-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:NP483477.RAzOeixTAlwEWmZmSxiFSjAyhVHRKPYzt6tBw_XvCOMX4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:49+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" .
}