@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4
> .
@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:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_head
{
this:
np:hasAssertion
dgn-np:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_assertion
;
np:hasProvenance
dgn-np:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_provenance
;
np:hasPublicationInfo
dgn-np:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_assertion
a
np:Assertion
.
dgn-np:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_provenance
a
np:Provenance
.
dgn-np:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNa8eb8c95c7bbcdf8e60243a6cbfbfe55
sio:SIO_000628
miriam-gene:4436
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_provenance
{
dgn-np:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_assertion
dcterms:description
"[Screening for germline MLH1, MSH2, MSH6, and PMS2 mutations was performed for all incident CRC cases recruited from cancer registries (population based probands) displaying microsatellite instability (MSI) or loss of expression of MMR genes by immunohistochemistry (IHC) and probands with CRC in multi-case families recruited from clinics (clinic based probands), regardless of MSI or IHC status.]. 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:21636617
;
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:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:53+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
> , <
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" .
}