@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k
> .
@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:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_head
{
this:
np:hasAssertion
dgn-np:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_assertion
;
np:hasProvenance
dgn-np:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_provenance
;
np:hasPublicationInfo
dgn-np:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_assertion
a
np:Assertion
.
dgn-np:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_provenance
a
np:Provenance
.
dgn-np:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGNbc2f2cf3c0b6522c4abc217a8478e860
sio:SIO_000628
miriam-gene:4436
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_provenance
{
dgn-np:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_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:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_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" .
}