@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP399302.RA9EzK35wC2SEYtpHxgu6ae-cvzhrHPvlVNJVJYhBGP6M
> .
@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:NP399302.RA9EzK35wC2SEYtpHxgu6ae-cvzhrHPvlVNJVJYhBGP6M130_head
{
this:
np:hasAssertion
dgn-np:NP399302.RA9EzK35wC2SEYtpHxgu6ae-cvzhrHPvlVNJVJYhBGP6M130_assertion
;
np:hasProvenance
dgn-np:NP399302.RA9EzK35wC2SEYtpHxgu6ae-cvzhrHPvlVNJVJYhBGP6M130_provenance
;
np:hasPublicationInfo
dgn-np:NP399302.RA9EzK35wC2SEYtpHxgu6ae-cvzhrHPvlVNJVJYhBGP6M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP399302.RA9EzK35wC2SEYtpHxgu6ae-cvzhrHPvlVNJVJYhBGP6M130_assertion
a
np:Assertion
.
dgn-np:NP399302.RA9EzK35wC2SEYtpHxgu6ae-cvzhrHPvlVNJVJYhBGP6M130_provenance
a
np:Provenance
.
dgn-np:NP399302.RA9EzK35wC2SEYtpHxgu6ae-cvzhrHPvlVNJVJYhBGP6M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP399302.RA9EzK35wC2SEYtpHxgu6ae-cvzhrHPvlVNJVJYhBGP6M130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C0265325
a
ncit:C7057
.
dgn-gda:DGNb4f1b6cf808aa793ac85a98074fb360b
sio:SIO_000628
miriam-gene:4436
,
lld:C0265325
;
a
sio:SIO_001121
.
}
dgn-np:NP399302.RA9EzK35wC2SEYtpHxgu6ae-cvzhrHPvlVNJVJYhBGP6M130_provenance
{
dgn-np:NP399302.RA9EzK35wC2SEYtpHxgu6ae-cvzhrHPvlVNJVJYhBGP6M130_assertion
dcterms:description
"[These data suggest the involvement of mismatch repair deficiency in the premalignant stage of tumorigenesis in HNPCC cases, and suggest that mismatch repair genes (MSH2 or others) are defective in the germline of nearly all these patients.]. 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:8137274
;
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:NP399302.RA9EzK35wC2SEYtpHxgu6ae-cvzhrHPvlVNJVJYhBGP6M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:58+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" .
}