@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP391981.RAG-oEGrv3ZQSivJftq73jbm76K_OeJiaL9KQu3sT4xOo
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP391981.RAG-oEGrv3ZQSivJftq73jbm76K_OeJiaL9KQu3sT4xOo130_assertion
;
np:hasProvenance
dgn-np:NP391981.RAG-oEGrv3ZQSivJftq73jbm76K_OeJiaL9KQu3sT4xOo130_provenance
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np:hasPublicationInfo
dgn-np:NP391981.RAG-oEGrv3ZQSivJftq73jbm76K_OeJiaL9KQu3sT4xOo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP391981.RAG-oEGrv3ZQSivJftq73jbm76K_OeJiaL9KQu3sT4xOo130_assertion
a
np:Assertion
.
dgn-np:NP391981.RAG-oEGrv3ZQSivJftq73jbm76K_OeJiaL9KQu3sT4xOo130_provenance
a
np:Provenance
.
dgn-np:NP391981.RAG-oEGrv3ZQSivJftq73jbm76K_OeJiaL9KQu3sT4xOo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP391981.RAG-oEGrv3ZQSivJftq73jbm76K_OeJiaL9KQu3sT4xOo130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C0001430
a
ncit:C7057
.
dgn-gda:DGN8f7bdf85d0be009dff66aac8946d4613
sio:SIO_000628
miriam-gene:4292
,
lld:C0001430
;
a
sio:SIO_001121
.
}
dgn-np:NP391981.RAG-oEGrv3ZQSivJftq73jbm76K_OeJiaL9KQu3sT4xOo130_provenance
{
dgn-np:NP391981.RAG-oEGrv3ZQSivJftq73jbm76K_OeJiaL9KQu3sT4xOo130_assertion
dcterms:description
"[This result is consistent with the finding that normal cells in HNPCC subjects are DNA repair proficient and supports the view that the mutational effects of the HNPCC gene occur selectively within adenomatous epithelium and serve to accelerate the adenoma-carcinoma sequence.]. 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:7892041
;
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:NP391981.RAG-oEGrv3ZQSivJftq73jbm76K_OeJiaL9KQu3sT4xOo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:53+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
> , <
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> , <
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" .
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