@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP181951.RAu8Vjw2ggwt9QFfzYqqDxPUbY8pvWbITnMVK28qlJdCU
> .
@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:NP181951.RAu8Vjw2ggwt9QFfzYqqDxPUbY8pvWbITnMVK28qlJdCU130_head
{
this:
np:hasAssertion
dgn-np:NP181951.RAu8Vjw2ggwt9QFfzYqqDxPUbY8pvWbITnMVK28qlJdCU130_assertion
;
np:hasProvenance
dgn-np:NP181951.RAu8Vjw2ggwt9QFfzYqqDxPUbY8pvWbITnMVK28qlJdCU130_provenance
;
np:hasPublicationInfo
dgn-np:NP181951.RAu8Vjw2ggwt9QFfzYqqDxPUbY8pvWbITnMVK28qlJdCU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP181951.RAu8Vjw2ggwt9QFfzYqqDxPUbY8pvWbITnMVK28qlJdCU130_assertion
a
np:Assertion
.
dgn-np:NP181951.RAu8Vjw2ggwt9QFfzYqqDxPUbY8pvWbITnMVK28qlJdCU130_provenance
a
np:Provenance
.
dgn-np:NP181951.RAu8Vjw2ggwt9QFfzYqqDxPUbY8pvWbITnMVK28qlJdCU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP181951.RAu8Vjw2ggwt9QFfzYqqDxPUbY8pvWbITnMVK28qlJdCU130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGNe1793cc728f5eafe20c5d679a2c6dfd0
sio:SIO_000628
miriam-gene:4292
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP181951.RAu8Vjw2ggwt9QFfzYqqDxPUbY8pvWbITnMVK28qlJdCU130_provenance
{
dgn-np:NP181951.RAu8Vjw2ggwt9QFfzYqqDxPUbY8pvWbITnMVK28qlJdCU130_assertion
dcterms:description
"[No apparent correlation was found between MSI and aneuploidy, whereas the immunohistochemical (IHC) analysis revealed that inactivation of the MLH1 mismatch repair gene may be involved in the majority of the MSI+ sporadic ECs.]. 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:12175698
;
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:NP181951.RAu8Vjw2ggwt9QFfzYqqDxPUbY8pvWbITnMVK28qlJdCU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:38+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" .
}