@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4
> .
@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:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_head
{
this:
np:hasAssertion
dgn-np:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_assertion
;
np:hasProvenance
dgn-np:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_provenance
;
np:hasPublicationInfo
dgn-np:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_assertion
a
np:Assertion
.
dgn-np:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_provenance
a
np:Provenance
.
dgn-np:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_assertion
{
miriam-gene:864
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGNc1b1ef5a413f2362bc73981e4f1d47ff
sio:SIO_000628
miriam-gene:864
,
lld:C0242379
;
a
sio:SIO_001121
.
}
dgn-np:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_provenance
{
dgn-np:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_assertion
dcterms:description
"[These results indicated that silencing of the RUNX3 gene plays an important role in the pathogenesis of lung cancer, and aberrant methylation is an important mechanism of inactivation of the RUNX3 gene in lung AdC.]. 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:16328045
;
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:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:49+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" .
}