@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP491954.RAHRyR58EceOgwzf62kfk53zUi1E7myKL2uo9E6ZQiMng
> .
@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:NP491954.RAHRyR58EceOgwzf62kfk53zUi1E7myKL2uo9E6ZQiMng130_head
{
this:
np:hasAssertion
dgn-np:NP491954.RAHRyR58EceOgwzf62kfk53zUi1E7myKL2uo9E6ZQiMng130_assertion
;
np:hasProvenance
dgn-np:NP491954.RAHRyR58EceOgwzf62kfk53zUi1E7myKL2uo9E6ZQiMng130_provenance
;
np:hasPublicationInfo
dgn-np:NP491954.RAHRyR58EceOgwzf62kfk53zUi1E7myKL2uo9E6ZQiMng130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP491954.RAHRyR58EceOgwzf62kfk53zUi1E7myKL2uo9E6ZQiMng130_assertion
a
np:Assertion
.
dgn-np:NP491954.RAHRyR58EceOgwzf62kfk53zUi1E7myKL2uo9E6ZQiMng130_provenance
a
np:Provenance
.
dgn-np:NP491954.RAHRyR58EceOgwzf62kfk53zUi1E7myKL2uo9E6ZQiMng130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP491954.RAHRyR58EceOgwzf62kfk53zUi1E7myKL2uo9E6ZQiMng130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGNd75cf670a295567dda4f7198b537758f
sio:SIO_000628
miriam-gene:4292
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP491954.RAHRyR58EceOgwzf62kfk53zUi1E7myKL2uo9E6ZQiMng130_provenance
{
dgn-np:NP491954.RAHRyR58EceOgwzf62kfk53zUi1E7myKL2uo9E6ZQiMng130_assertion
dcterms:description
"[A significant fraction of hereditary nonpolyposis colorectal cancer cases with defective mismatch repair (ie, Lynch syndrome) have large genomic deletions or duplications in the mismatch repair genes, hMLH1 and hMSH2, which can be challenging to detect by traditional methods.]. 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:15858146
;
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:NP491954.RAHRyR58EceOgwzf62kfk53zUi1E7myKL2uo9E6ZQiMng130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:28+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" .
}