@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP285503.RA9t8PCnJekcuqyBjp3V6B0toaUa5FV_ZHlyQcTrOIiS4
> .
@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:NP285503.RA9t8PCnJekcuqyBjp3V6B0toaUa5FV_ZHlyQcTrOIiS4130_head
{
this:
np:hasAssertion
dgn-np:NP285503.RA9t8PCnJekcuqyBjp3V6B0toaUa5FV_ZHlyQcTrOIiS4130_assertion
;
np:hasProvenance
dgn-np:NP285503.RA9t8PCnJekcuqyBjp3V6B0toaUa5FV_ZHlyQcTrOIiS4130_provenance
;
np:hasPublicationInfo
dgn-np:NP285503.RA9t8PCnJekcuqyBjp3V6B0toaUa5FV_ZHlyQcTrOIiS4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP285503.RA9t8PCnJekcuqyBjp3V6B0toaUa5FV_ZHlyQcTrOIiS4130_assertion
a
np:Assertion
.
dgn-np:NP285503.RA9t8PCnJekcuqyBjp3V6B0toaUa5FV_ZHlyQcTrOIiS4130_provenance
a
np:Provenance
.
dgn-np:NP285503.RA9t8PCnJekcuqyBjp3V6B0toaUa5FV_ZHlyQcTrOIiS4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP285503.RA9t8PCnJekcuqyBjp3V6B0toaUa5FV_ZHlyQcTrOIiS4130_assertion
{
miriam-gene:4361
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGN4ab37a16c6c457a7046b6495d9ac2c22
sio:SIO_000628
miriam-gene:4361
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP285503.RA9t8PCnJekcuqyBjp3V6B0toaUa5FV_ZHlyQcTrOIiS4130_provenance
{
dgn-np:NP285503.RA9t8PCnJekcuqyBjp3V6B0toaUa5FV_ZHlyQcTrOIiS4130_assertion
dcterms:description
"[Immunohistochemistry (MLH1, MSH2, MSH6) showed that loss of mismatch repair protein expression occurred in all MSI UUC defining the gene defect and that MRE11 and RAD50 mutations were associated with their concomitant loss expression.]. 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:16288216
;
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:NP285503.RA9t8PCnJekcuqyBjp3V6B0toaUa5FV_ZHlyQcTrOIiS4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:41+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" .
}