@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP228281.RAp8i8IWyKvx54dWYuQQhKuPldTZY4YWsasMB038dR-Ak
> .
@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:NP228281.RAp8i8IWyKvx54dWYuQQhKuPldTZY4YWsasMB038dR-Ak130_head
{
this:
np:hasAssertion
dgn-np:NP228281.RAp8i8IWyKvx54dWYuQQhKuPldTZY4YWsasMB038dR-Ak130_assertion
;
np:hasProvenance
dgn-np:NP228281.RAp8i8IWyKvx54dWYuQQhKuPldTZY4YWsasMB038dR-Ak130_provenance
;
np:hasPublicationInfo
dgn-np:NP228281.RAp8i8IWyKvx54dWYuQQhKuPldTZY4YWsasMB038dR-Ak130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP228281.RAp8i8IWyKvx54dWYuQQhKuPldTZY4YWsasMB038dR-Ak130_assertion
a
np:Assertion
.
dgn-np:NP228281.RAp8i8IWyKvx54dWYuQQhKuPldTZY4YWsasMB038dR-Ak130_provenance
a
np:Provenance
.
dgn-np:NP228281.RAp8i8IWyKvx54dWYuQQhKuPldTZY4YWsasMB038dR-Ak130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP228281.RAp8i8IWyKvx54dWYuQQhKuPldTZY4YWsasMB038dR-Ak130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0001418
a
ncit:C7057
.
dgn-gda:DGN06ebe3339f725caceecab8c86c12cfa3
sio:SIO_000628
miriam-gene:3342
,
lld:C0001418
;
a
sio:SIO_001121
.
}
dgn-np:NP228281.RAp8i8IWyKvx54dWYuQQhKuPldTZY4YWsasMB038dR-Ak130_provenance
{
dgn-np:NP228281.RAp8i8IWyKvx54dWYuQQhKuPldTZY4YWsasMB038dR-Ak130_assertion
dcterms:description
"[To clarify the clinicopathological and biological significance of genomic alterations in pulmonary adenocarcinomas, we examined chromosomal DNA sequence copy number aberrations (DSCNAs) and DNA ploidy in 42 surgically resected specimens by comparative genomic hybridization (CGH) and laser scanning cytometry (LSC), respectively.]. 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:16273235
;
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:NP228281.RAp8i8IWyKvx54dWYuQQhKuPldTZY4YWsasMB038dR-Ak130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:08+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" .
}