@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE
> .
@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:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_head
{
this:
np:hasAssertion
dgn-np:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_assertion
;
np:hasProvenance
dgn-np:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_provenance
;
np:hasPublicationInfo
dgn-np:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_assertion
a
np:Assertion
.
dgn-np:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_provenance
a
np:Provenance
.
dgn-np:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0007131
a
ncit:C7057
.
dgn-gda:DGN2fc2372b0c8d04380c4efb9bfaff6c0d
sio:SIO_000628
miriam-gene:3342
,
lld:C0007131
;
a
sio:SIO_001121
.
}
dgn-np:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_provenance
{
dgn-np:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_assertion
dcterms:description
"[To identify early-stage genetic events that drive progression of NSCLC, we conducted a high-resolution array comparative genomic hybridization (CGH) study, using an array of 4,046 bacterial artificial chromosome clones to screen for DNA copy number changes associated with individual genes in 36 tumors obtained from patients in early stages of NSCLC.]. 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:18328944
;
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:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:16+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" .
}