@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1401560.RAVxd4rL8VFPhdLB_mKhWYFz2HNhUwM3LIJrA53YE49mE
> .
@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:NP1401560.RAVxd4rL8VFPhdLB_mKhWYFz2HNhUwM3LIJrA53YE49mE130_head
{
this:
np:hasAssertion
dgn-np:NP1401560.RAVxd4rL8VFPhdLB_mKhWYFz2HNhUwM3LIJrA53YE49mE130_assertion
;
np:hasProvenance
dgn-np:NP1401560.RAVxd4rL8VFPhdLB_mKhWYFz2HNhUwM3LIJrA53YE49mE130_provenance
;
np:hasPublicationInfo
dgn-np:NP1401560.RAVxd4rL8VFPhdLB_mKhWYFz2HNhUwM3LIJrA53YE49mE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1401560.RAVxd4rL8VFPhdLB_mKhWYFz2HNhUwM3LIJrA53YE49mE130_assertion
a
np:Assertion
.
dgn-np:NP1401560.RAVxd4rL8VFPhdLB_mKhWYFz2HNhUwM3LIJrA53YE49mE130_provenance
a
np:Provenance
.
dgn-np:NP1401560.RAVxd4rL8VFPhdLB_mKhWYFz2HNhUwM3LIJrA53YE49mE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1401560.RAVxd4rL8VFPhdLB_mKhWYFz2HNhUwM3LIJrA53YE49mE130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN28fc247af95f1d546fae7c790f1154af
sio:SIO_000628
miriam-gene:4292
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP1401560.RAVxd4rL8VFPhdLB_mKhWYFz2HNhUwM3LIJrA53YE49mE130_provenance
{
dgn-np:NP1401560.RAVxd4rL8VFPhdLB_mKhWYFz2HNhUwM3LIJrA53YE49mE130_assertion
dcterms:description
"[Although defective mismatch repair, consisting primarily of alterations in hMSH2 and hMLH1, is believed to be responsible for the MSI phenotype in the majority of patients with hereditary nonpolyposis colon cancer, the genetic defect responsible for this phenotype in sporadic CRC has yet to be clearly delineated.]. 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:9699680
;
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:NP1401560.RAVxd4rL8VFPhdLB_mKhWYFz2HNhUwM3LIJrA53YE49mE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:21+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" .
}