@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP244316.RAjbptEQR2eda9ysyF2Oj52I0CgqDYiZD2mtoK_Mov9RI
> .
@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:NP244316.RAjbptEQR2eda9ysyF2Oj52I0CgqDYiZD2mtoK_Mov9RI130_head
{
this:
np:hasAssertion
dgn-np:NP244316.RAjbptEQR2eda9ysyF2Oj52I0CgqDYiZD2mtoK_Mov9RI130_assertion
;
np:hasProvenance
dgn-np:NP244316.RAjbptEQR2eda9ysyF2Oj52I0CgqDYiZD2mtoK_Mov9RI130_provenance
;
np:hasPublicationInfo
dgn-np:NP244316.RAjbptEQR2eda9ysyF2Oj52I0CgqDYiZD2mtoK_Mov9RI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP244316.RAjbptEQR2eda9ysyF2Oj52I0CgqDYiZD2mtoK_Mov9RI130_assertion
a
np:Assertion
.
dgn-np:NP244316.RAjbptEQR2eda9ysyF2Oj52I0CgqDYiZD2mtoK_Mov9RI130_provenance
a
np:Provenance
.
dgn-np:NP244316.RAjbptEQR2eda9ysyF2Oj52I0CgqDYiZD2mtoK_Mov9RI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP244316.RAjbptEQR2eda9ysyF2Oj52I0CgqDYiZD2mtoK_Mov9RI130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN495b5e67d236b395438c6961c8bf8023
sio:SIO_000628
miriam-gene:5624
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP244316.RAjbptEQR2eda9ysyF2Oj52I0CgqDYiZD2mtoK_Mov9RI130_provenance
{
dgn-np:NP244316.RAjbptEQR2eda9ysyF2Oj52I0CgqDYiZD2mtoK_Mov9RI130_assertion
dcterms:description
"[These findings suggest that the genetic instability that is reflected by the RER phenotype precedes, and is responsible for, APC mutation in RER large bowel tumors and have important implications for understanding the very earliest stages of neoplasia in patients with tumors deficient in mismatch repair.]. 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:8799152
;
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:NP244316.RAjbptEQR2eda9ysyF2Oj52I0CgqDYiZD2mtoK_Mov9RI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:16+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" .
}