@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM
> .
@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:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_head
{
this:
np:hasAssertion
dgn-np:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_assertion
;
np:hasProvenance
dgn-np:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_provenance
;
np:hasPublicationInfo
dgn-np:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_assertion
a
np:Assertion
.
dgn-np:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_provenance
a
np:Provenance
.
dgn-np:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN53bb5ab7ace417fb37bd1cde7a41d262
sio:SIO_000628
miriam-gene:4360
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_provenance
{
dgn-np:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_assertion
dcterms:description
"[Carcinomas of the small intestine are rare, but the risk is greatly increased in patients with hereditary nonpolyposis colorectal cancer (HNPCC) due to an inherited mismatch repair (MMR) gene mutation, most commonly affecting the genes MLH1 or MSH2.]. 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:12627520
;
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:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:40+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" .
}