@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP921541.RApHLGYDRktEgGuWaDtqr34RMXkax603t8Nx8UCnzHDb4
> .
@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:NP921541.RApHLGYDRktEgGuWaDtqr34RMXkax603t8Nx8UCnzHDb4130_head
{
this:
np:hasAssertion
dgn-np:NP921541.RApHLGYDRktEgGuWaDtqr34RMXkax603t8Nx8UCnzHDb4130_assertion
;
np:hasProvenance
dgn-np:NP921541.RApHLGYDRktEgGuWaDtqr34RMXkax603t8Nx8UCnzHDb4130_provenance
;
np:hasPublicationInfo
dgn-np:NP921541.RApHLGYDRktEgGuWaDtqr34RMXkax603t8Nx8UCnzHDb4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP921541.RApHLGYDRktEgGuWaDtqr34RMXkax603t8Nx8UCnzHDb4130_assertion
a
np:Assertion
.
dgn-np:NP921541.RApHLGYDRktEgGuWaDtqr34RMXkax603t8Nx8UCnzHDb4130_provenance
a
np:Provenance
.
dgn-np:NP921541.RApHLGYDRktEgGuWaDtqr34RMXkax603t8Nx8UCnzHDb4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP921541.RApHLGYDRktEgGuWaDtqr34RMXkax603t8Nx8UCnzHDb4130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C0007129
a
ncit:C7057
.
dgn-gda:DGN8a3a8b01f4542b901cf561ced16f7a94
sio:SIO_000628
miriam-gene:673
,
lld:C0007129
;
a
sio:SIO_001121
.
}
dgn-np:NP921541.RApHLGYDRktEgGuWaDtqr34RMXkax603t8Nx8UCnzHDb4130_provenance
{
dgn-np:NP921541.RApHLGYDRktEgGuWaDtqr34RMXkax603t8Nx8UCnzHDb4130_assertion
dcterms:description
"[We show MCC expression is dramatically decreased in many CRC cell lines and the distinct subset of sporadic CRC characterized by the CpG island methylator phenotype and BRAF(V600E) mutation due to promoter methylation as reported previously.]. 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:18591935
;
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:NP921541.RApHLGYDRktEgGuWaDtqr34RMXkax603t8Nx8UCnzHDb4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:25+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" .
}