@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP463698.RALFm-Ym0w9gZqJeFjVXYs5aBASNsETPSL0umRPhCybsI
> .
@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:NP463698.RALFm-Ym0w9gZqJeFjVXYs5aBASNsETPSL0umRPhCybsI130_head
{
this:
np:hasAssertion
dgn-np:NP463698.RALFm-Ym0w9gZqJeFjVXYs5aBASNsETPSL0umRPhCybsI130_assertion
;
np:hasProvenance
dgn-np:NP463698.RALFm-Ym0w9gZqJeFjVXYs5aBASNsETPSL0umRPhCybsI130_provenance
;
np:hasPublicationInfo
dgn-np:NP463698.RALFm-Ym0w9gZqJeFjVXYs5aBASNsETPSL0umRPhCybsI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP463698.RALFm-Ym0w9gZqJeFjVXYs5aBASNsETPSL0umRPhCybsI130_assertion
a
np:Assertion
.
dgn-np:NP463698.RALFm-Ym0w9gZqJeFjVXYs5aBASNsETPSL0umRPhCybsI130_provenance
a
np:Provenance
.
dgn-np:NP463698.RALFm-Ym0w9gZqJeFjVXYs5aBASNsETPSL0umRPhCybsI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP463698.RALFm-Ym0w9gZqJeFjVXYs5aBASNsETPSL0umRPhCybsI130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0029463
a
ncit:C7057
.
dgn-gda:DGNbfa60445202dd2ad7699ff90eadd19bc
sio:SIO_000628
miriam-gene:3342
,
lld:C0029463
;
a
sio:SIO_001121
.
}
dgn-np:NP463698.RALFm-Ym0w9gZqJeFjVXYs5aBASNsETPSL0umRPhCybsI130_provenance
{
dgn-np:NP463698.RALFm-Ym0w9gZqJeFjVXYs5aBASNsETPSL0umRPhCybsI130_assertion
dcterms:description
"[This genome wide analysis is the first utilizing oligonucleotide array CGH in combination with FISH analysis to derive genomic signatures of chromosomal instability in OS tumors by studying genomic imbalance and intercellular heterogeneity.]. 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:18931480
;
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:NP463698.RALFm-Ym0w9gZqJeFjVXYs5aBASNsETPSL0umRPhCybsI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:36+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" .
}