@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP477978.RAGwAudBRPnFDNhYIXveza8uPB6AaTICPcufAQM_O9PuU
> .
@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:NP477978.RAGwAudBRPnFDNhYIXveza8uPB6AaTICPcufAQM_O9PuU130_head
{
this:
np:hasAssertion
dgn-np:NP477978.RAGwAudBRPnFDNhYIXveza8uPB6AaTICPcufAQM_O9PuU130_assertion
;
np:hasProvenance
dgn-np:NP477978.RAGwAudBRPnFDNhYIXveza8uPB6AaTICPcufAQM_O9PuU130_provenance
;
np:hasPublicationInfo
dgn-np:NP477978.RAGwAudBRPnFDNhYIXveza8uPB6AaTICPcufAQM_O9PuU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP477978.RAGwAudBRPnFDNhYIXveza8uPB6AaTICPcufAQM_O9PuU130_assertion
a
np:Assertion
.
dgn-np:NP477978.RAGwAudBRPnFDNhYIXveza8uPB6AaTICPcufAQM_O9PuU130_provenance
a
np:Provenance
.
dgn-np:NP477978.RAGwAudBRPnFDNhYIXveza8uPB6AaTICPcufAQM_O9PuU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP477978.RAGwAudBRPnFDNhYIXveza8uPB6AaTICPcufAQM_O9PuU130_assertion
{
miriam-gene:1012
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNc929ebfd399ba550cb7cb4db6ae37ba9
sio:SIO_000628
miriam-gene:1012
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP477978.RAGwAudBRPnFDNhYIXveza8uPB6AaTICPcufAQM_O9PuU130_provenance
{
dgn-np:NP477978.RAGwAudBRPnFDNhYIXveza8uPB6AaTICPcufAQM_O9PuU130_assertion
dcterms:description
"[This result suggested that poorly differentiated colorectal cancers specifically exhibited CDH13 methylation, and since CDH13 might be responsible for selective cell recognition and adhesion, inactivation of CDH13 could lead to the formation of scattered carcinoma cells in these cancers.]. 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:14997203
;
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:NP477978.RAGwAudBRPnFDNhYIXveza8uPB6AaTICPcufAQM_O9PuU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:46+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" .
}