@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU
> .
@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/v3.0.0/void/
> .
dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_head
{
this:
np:hasAssertion
dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_assertion
;
np:hasProvenance
dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_provenance
;
np:hasPublicationInfo
dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_assertion
a
np:Assertion
.
dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_provenance
a
np:Provenance
.
dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C1306459
a
ncit:C7057
.
dgn-gda:DGNf0d84fe691a71853f5566ac98c41dc5d
sio:SIO_000628
miriam-gene:4360
,
lld:C1306459
;
a
sio:SIO_001121
.
}
dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_provenance
{
dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_assertion
dcterms:description
"[In many individuals suspected of the common cancer predisposition Lynch syndrome, variants of unclear significance (VUS), rather than an obviously pathogenic mutations, are identified in one of the DNA mismatch repair (MMR) genes.]. 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:23690608
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:18+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}