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http://rdf.disgenet.org/nanopublications.trig#NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk
> .
@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:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_head
{
this:
np:hasAssertion
dgn-np:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_assertion
;
np:hasProvenance
dgn-np:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_provenance
;
np:hasPublicationInfo
dgn-np:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_assertion
a
np:Assertion
.
dgn-np:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_provenance
a
np:Provenance
.
dgn-np:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_assertion
{
miriam-gene:54361
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGNecffbe2149766c0b69a73f5d73b94e25
sio:SIO_000628
miriam-gene:54361
,
lld:C0242379
;
a
sio:SIO_001121
.
}
dgn-np:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_provenance
{
dgn-np:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_assertion
dcterms:description
"[Our finding of a 0.4 Mb amplified region at 1p36.12 containing WNT4 in preinvasive lung cancer, coupled with the identification of three additional alterations in invasive tumors that also contain genes related to the Notch and Wnt pathways, strongly suggests an intricate role of these pathways in early and late stages of lung cancer development.]. 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:15615770
;
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 .
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dgn-np:NP583277.RA6fmELnz6fEAtlzdAfHEBn4xaFnb99XlQZXBlU7Id-hk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:51+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
<
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> , <
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
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dgn-void:disgenetrdf
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"v2.1.0" .
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