@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP314109.RARs1xnYTLDBrqybzuqFzSl_eg0_Ws_cff9Y2DKUZcncA
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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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#
> .
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{
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np:hasAssertion
dgn-np:NP314109.RARs1xnYTLDBrqybzuqFzSl_eg0_Ws_cff9Y2DKUZcncA130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP314109.RARs1xnYTLDBrqybzuqFzSl_eg0_Ws_cff9Y2DKUZcncA130_publicationInfo
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a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP314109.RARs1xnYTLDBrqybzuqFzSl_eg0_Ws_cff9Y2DKUZcncA130_provenance
a
np:Provenance
.
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np:PublicationInfo
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{
miriam-gene:4092
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN1b8453e267a594306502f9e629f5ba43
sio:SIO_000628
miriam-gene:4092
,
lld:C1527249
;
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.
}
dgn-np:NP314109.RARs1xnYTLDBrqybzuqFzSl_eg0_Ws_cff9Y2DKUZcncA130_provenance
{
dgn-np:NP314109.RARs1xnYTLDBrqybzuqFzSl_eg0_Ws_cff9Y2DKUZcncA130_assertion
dcterms:description
"[These findings suggest that individuals with this SMAD7 variant that develop CRC are more probably to have tumors with greater invasiveness and methylation of RUNX3, which potentially contributes to their poorer observed survival.]. 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:23104301
;
prov:wasDerivedFrom
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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 .
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dgn-np:NP314109.RARs1xnYTLDBrqybzuqFzSl_eg0_Ws_cff9Y2DKUZcncA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:00+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
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pav:authoredBy
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> , <
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> ;
pav:createdBy
<
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