@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP395774.RA2l-ZMKJIz9hzdDydHnP9dMuKuixLNyf1h0ahYlwwaT0
> .
@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:NP395774.RA2l-ZMKJIz9hzdDydHnP9dMuKuixLNyf1h0ahYlwwaT0130_head
{
this:
np:hasAssertion
dgn-np:NP395774.RA2l-ZMKJIz9hzdDydHnP9dMuKuixLNyf1h0ahYlwwaT0130_assertion
;
np:hasProvenance
dgn-np:NP395774.RA2l-ZMKJIz9hzdDydHnP9dMuKuixLNyf1h0ahYlwwaT0130_provenance
;
np:hasPublicationInfo
dgn-np:NP395774.RA2l-ZMKJIz9hzdDydHnP9dMuKuixLNyf1h0ahYlwwaT0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP395774.RA2l-ZMKJIz9hzdDydHnP9dMuKuixLNyf1h0ahYlwwaT0130_assertion
a
np:Assertion
.
dgn-np:NP395774.RA2l-ZMKJIz9hzdDydHnP9dMuKuixLNyf1h0ahYlwwaT0130_provenance
a
np:Provenance
.
dgn-np:NP395774.RA2l-ZMKJIz9hzdDydHnP9dMuKuixLNyf1h0ahYlwwaT0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP395774.RA2l-ZMKJIz9hzdDydHnP9dMuKuixLNyf1h0ahYlwwaT0130_assertion
{
miriam-gene:864
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGN88933060c0612642bb38fd103db48b70
sio:SIO_000628
miriam-gene:864
,
lld:C0596263
;
a
sio:SIO_001121
.
}
dgn-np:NP395774.RA2l-ZMKJIz9hzdDydHnP9dMuKuixLNyf1h0ahYlwwaT0130_provenance
{
dgn-np:NP395774.RA2l-ZMKJIz9hzdDydHnP9dMuKuixLNyf1h0ahYlwwaT0130_assertion
dcterms:description
"[To verify the genetic alterations and methylation status of the RUNX3 gene in colorectal carcinogenesis, we analysed for mutations, loss of heterozygosity (LOH), and RUNX3 gene promoter hypermethylation, in 32 colorectal cancer cell lines.]. 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:15273736
;
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:NP395774.RA2l-ZMKJIz9hzdDydHnP9dMuKuixLNyf1h0ahYlwwaT0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:55+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" .
}