@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1112151.RANgHzfVu8YAOK-7LGps2jx7CtO2BQCTry5A7l9xdwr6I
> .
@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:NP1112151.RANgHzfVu8YAOK-7LGps2jx7CtO2BQCTry5A7l9xdwr6I130_head
{
this:
np:hasAssertion
dgn-np:NP1112151.RANgHzfVu8YAOK-7LGps2jx7CtO2BQCTry5A7l9xdwr6I130_assertion
;
np:hasProvenance
dgn-np:NP1112151.RANgHzfVu8YAOK-7LGps2jx7CtO2BQCTry5A7l9xdwr6I130_provenance
;
np:hasPublicationInfo
dgn-np:NP1112151.RANgHzfVu8YAOK-7LGps2jx7CtO2BQCTry5A7l9xdwr6I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1112151.RANgHzfVu8YAOK-7LGps2jx7CtO2BQCTry5A7l9xdwr6I130_assertion
a
np:Assertion
.
dgn-np:NP1112151.RANgHzfVu8YAOK-7LGps2jx7CtO2BQCTry5A7l9xdwr6I130_provenance
a
np:Provenance
.
dgn-np:NP1112151.RANgHzfVu8YAOK-7LGps2jx7CtO2BQCTry5A7l9xdwr6I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1112151.RANgHzfVu8YAOK-7LGps2jx7CtO2BQCTry5A7l9xdwr6I130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0265325
a
ncit:C7057
.
dgn-gda:DGN216ac231ce6acbe3e857752118a85608
sio:SIO_000628
miriam-gene:4360
,
lld:C0265325
;
a
sio:SIO_001121
.
}
dgn-np:NP1112151.RANgHzfVu8YAOK-7LGps2jx7CtO2BQCTry5A7l9xdwr6I130_provenance
{
dgn-np:NP1112151.RANgHzfVu8YAOK-7LGps2jx7CtO2BQCTry5A7l9xdwr6I130_assertion
dcterms:description
"[Patients who carry either single allele (LS) or double allele (constitutional mismatch repair deficiency syndrome) mutations in the MMR genes benefit from cancer surveillance programs that target both the digestive and extraintestinal cancer risk of these diseases.]. 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:24051481
;
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:NP1112151.RANgHzfVu8YAOK-7LGps2jx7CtO2BQCTry5A7l9xdwr6I130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:10+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" .
}