@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP799289.RAg8hiWL62340MxOqG2War5MiPSIDtG8NS7-OpjozBczc
> .
@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:NP799289.RAg8hiWL62340MxOqG2War5MiPSIDtG8NS7-OpjozBczc130_head
{
this:
np:hasAssertion
dgn-np:NP799289.RAg8hiWL62340MxOqG2War5MiPSIDtG8NS7-OpjozBczc130_assertion
;
np:hasProvenance
dgn-np:NP799289.RAg8hiWL62340MxOqG2War5MiPSIDtG8NS7-OpjozBczc130_provenance
;
np:hasPublicationInfo
dgn-np:NP799289.RAg8hiWL62340MxOqG2War5MiPSIDtG8NS7-OpjozBczc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP799289.RAg8hiWL62340MxOqG2War5MiPSIDtG8NS7-OpjozBczc130_assertion
a
np:Assertion
.
dgn-np:NP799289.RAg8hiWL62340MxOqG2War5MiPSIDtG8NS7-OpjozBczc130_provenance
a
np:Provenance
.
dgn-np:NP799289.RAg8hiWL62340MxOqG2War5MiPSIDtG8NS7-OpjozBczc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP799289.RAg8hiWL62340MxOqG2War5MiPSIDtG8NS7-OpjozBczc130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0007130
a
ncit:C7057
.
dgn-gda:DGNb161be441eed2d6ddf23b921828e5f0d
sio:SIO_000628
miriam-gene:3342
,
lld:C0007130
;
a
sio:SIO_001121
.
}
dgn-np:NP799289.RAg8hiWL62340MxOqG2War5MiPSIDtG8NS7-OpjozBczc130_provenance
{
dgn-np:NP799289.RAg8hiWL62340MxOqG2War5MiPSIDtG8NS7-OpjozBczc130_assertion
dcterms:description
"[The overall pattern of chromosomal changes detected by spectral karyotype (SKY) analysis of two cell lines of each major histological subtype of NSCLC, namely squamous cell carcinoma (SQCC) and adenocarcinoma (ADC), indicated a greater degree of chromosomal rearrangement, than was present or predicted by either comparative genomic hybridization (CGH) or G-banding analysis alone.]. 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:11369051
;
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:NP799289.RAg8hiWL62340MxOqG2War5MiPSIDtG8NS7-OpjozBczc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:10+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" .
}