@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP837805.RAS9lN6VGbqMjfCut7I1_lu-p3jRSZD27bCFzHX3uit8k
> .
@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:NP837805.RAS9lN6VGbqMjfCut7I1_lu-p3jRSZD27bCFzHX3uit8k130_head
{
this:
np:hasAssertion
dgn-np:NP837805.RAS9lN6VGbqMjfCut7I1_lu-p3jRSZD27bCFzHX3uit8k130_assertion
;
np:hasProvenance
dgn-np:NP837805.RAS9lN6VGbqMjfCut7I1_lu-p3jRSZD27bCFzHX3uit8k130_provenance
;
np:hasPublicationInfo
dgn-np:NP837805.RAS9lN6VGbqMjfCut7I1_lu-p3jRSZD27bCFzHX3uit8k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP837805.RAS9lN6VGbqMjfCut7I1_lu-p3jRSZD27bCFzHX3uit8k130_assertion
a
np:Assertion
.
dgn-np:NP837805.RAS9lN6VGbqMjfCut7I1_lu-p3jRSZD27bCFzHX3uit8k130_provenance
a
np:Provenance
.
dgn-np:NP837805.RAS9lN6VGbqMjfCut7I1_lu-p3jRSZD27bCFzHX3uit8k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP837805.RAS9lN6VGbqMjfCut7I1_lu-p3jRSZD27bCFzHX3uit8k130_assertion
{
miriam-gene:3181
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGN95e12630fa66bffffec211ce6c9a9f66
sio:SIO_000628
miriam-gene:3181
,
lld:C0242379
;
a
sio:SIO_001121
.
}
dgn-np:NP837805.RAS9lN6VGbqMjfCut7I1_lu-p3jRSZD27bCFzHX3uit8k130_provenance
{
dgn-np:NP837805.RAS9lN6VGbqMjfCut7I1_lu-p3jRSZD27bCFzHX3uit8k130_assertion
dcterms:description
"[Cytological atypia, bronchial metaplasia, protein (hnRNP A2/B1) overexpression, ras oncogene activation and tumour-suppressor gene deletion, genomic instability (loss of heterozygosity, microsatellite alterations), abnormal methylation, helical CT detection of atypical adenomatous hyperplasia and fluorescent bronchoscopic detection of angiogenic squamous dysplasia offer great promise for molecular diagnosis of lung cancer far in advance of clinical presentation.]. 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:11220665
;
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:NP837805.RAS9lN6VGbqMjfCut7I1_lu-p3jRSZD27bCFzHX3uit8k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:32+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" .
}