@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP890996.RA8htYcfqYGRjchg600alujU21M090EJYhr79HWG6B6uk
> .
@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:NP890996.RA8htYcfqYGRjchg600alujU21M090EJYhr79HWG6B6uk130_head
{
this:
np:hasAssertion
dgn-np:NP890996.RA8htYcfqYGRjchg600alujU21M090EJYhr79HWG6B6uk130_assertion
;
np:hasProvenance
dgn-np:NP890996.RA8htYcfqYGRjchg600alujU21M090EJYhr79HWG6B6uk130_provenance
;
np:hasPublicationInfo
dgn-np:NP890996.RA8htYcfqYGRjchg600alujU21M090EJYhr79HWG6B6uk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP890996.RA8htYcfqYGRjchg600alujU21M090EJYhr79HWG6B6uk130_assertion
a
np:Assertion
.
dgn-np:NP890996.RA8htYcfqYGRjchg600alujU21M090EJYhr79HWG6B6uk130_provenance
a
np:Provenance
.
dgn-np:NP890996.RA8htYcfqYGRjchg600alujU21M090EJYhr79HWG6B6uk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP890996.RA8htYcfqYGRjchg600alujU21M090EJYhr79HWG6B6uk130_assertion
{
miriam-gene:5395
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGN6caff3d5947ebad3117bd69e4983a71f
sio:SIO_000628
miriam-gene:5395
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP890996.RA8htYcfqYGRjchg600alujU21M090EJYhr79HWG6B6uk130_provenance
{
dgn-np:NP890996.RA8htYcfqYGRjchg600alujU21M090EJYhr79HWG6B6uk130_assertion
dcterms:description
"[In conclusion, our data outline the main scenarios where significant reduction of MSH6 staining is more likely to occur in colorectal carcinoma, and suggest that somatic mutations of the coding region microsatellites of the MSH6 gene is an underlying mechanism for this staining phenomenon in MLH1/PMS2-deficient carcinomas.]. 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:22918162
;
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:NP890996.RA8htYcfqYGRjchg600alujU21M090EJYhr79HWG6B6uk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:07+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" .
}