@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP156280.RAxzfeWGjdhGTcoPvtoQrkFtGji35OB4s7clDj4xOEvz4
> .
@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:NP156280.RAxzfeWGjdhGTcoPvtoQrkFtGji35OB4s7clDj4xOEvz4130_head
{
this:
np:hasAssertion
dgn-np:NP156280.RAxzfeWGjdhGTcoPvtoQrkFtGji35OB4s7clDj4xOEvz4130_assertion
;
np:hasProvenance
dgn-np:NP156280.RAxzfeWGjdhGTcoPvtoQrkFtGji35OB4s7clDj4xOEvz4130_provenance
;
np:hasPublicationInfo
dgn-np:NP156280.RAxzfeWGjdhGTcoPvtoQrkFtGji35OB4s7clDj4xOEvz4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP156280.RAxzfeWGjdhGTcoPvtoQrkFtGji35OB4s7clDj4xOEvz4130_assertion
a
np:Assertion
.
dgn-np:NP156280.RAxzfeWGjdhGTcoPvtoQrkFtGji35OB4s7clDj4xOEvz4130_provenance
a
np:Provenance
.
dgn-np:NP156280.RAxzfeWGjdhGTcoPvtoQrkFtGji35OB4s7clDj4xOEvz4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP156280.RAxzfeWGjdhGTcoPvtoQrkFtGji35OB4s7clDj4xOEvz4130_assertion
{
miriam-gene:4609
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGN723b634b5a61f54012d6257fa2139a2b
sio:SIO_000628
miriam-gene:4609
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP156280.RAxzfeWGjdhGTcoPvtoQrkFtGji35OB4s7clDj4xOEvz4130_provenance
{
dgn-np:NP156280.RAxzfeWGjdhGTcoPvtoQrkFtGji35OB4s7clDj4xOEvz4130_assertion
dcterms:description
"[In the following study, we used comparative genomic hybridization (CGH) to screen for DNA copy number changes along all chromosomes in 37 gastric carcinomas, and fluorescence in situ hybridization (FISH) with the C-MYC and TP53 probes in 14 cases for comparison.]. 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:10704677
;
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:NP156280.RAxzfeWGjdhGTcoPvtoQrkFtGji35OB4s7clDj4xOEvz4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:24+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" .
}