@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_head
{
this:
np:hasAssertion
dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_assertion
;
np:hasProvenance
dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_assertion
a
np:Assertion
.
dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_provenance
a
np:Provenance
.
dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGNd1f8aa5cf9615913fc4b36a3116bce19
sio:SIO_000628
miriam-gene:4436
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_provenance
{
dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_assertion
dcterms:description
"[Because the frequency of mutations in the mismatch repair genes (hMLH1 and hMSH2) is low in these tumors, we have investigated the role of mutational inactivation, methylation of the promoter region, and loss of heterozygosity (LOH) as a possible explanation for the mutator phenotype of RER+ colorectal cancer cell lines.]. 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:10468602
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:44+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}