@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1366019.RA4WEH2QP2PGsVsSZzWhC7rmSVFJq79u0tH3IBaImprY4
> .
@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:NP1366019.RA4WEH2QP2PGsVsSZzWhC7rmSVFJq79u0tH3IBaImprY4130_head
{
this:
np:hasAssertion
dgn-np:NP1366019.RA4WEH2QP2PGsVsSZzWhC7rmSVFJq79u0tH3IBaImprY4130_assertion
;
np:hasProvenance
dgn-np:NP1366019.RA4WEH2QP2PGsVsSZzWhC7rmSVFJq79u0tH3IBaImprY4130_provenance
;
np:hasPublicationInfo
dgn-np:NP1366019.RA4WEH2QP2PGsVsSZzWhC7rmSVFJq79u0tH3IBaImprY4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1366019.RA4WEH2QP2PGsVsSZzWhC7rmSVFJq79u0tH3IBaImprY4130_assertion
a
np:Assertion
.
dgn-np:NP1366019.RA4WEH2QP2PGsVsSZzWhC7rmSVFJq79u0tH3IBaImprY4130_provenance
a
np:Provenance
.
dgn-np:NP1366019.RA4WEH2QP2PGsVsSZzWhC7rmSVFJq79u0tH3IBaImprY4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1366019.RA4WEH2QP2PGsVsSZzWhC7rmSVFJq79u0tH3IBaImprY4130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN7551595156115cf7c4933f640b49fead
sio:SIO_000628
miriam-gene:4360
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP1366019.RA4WEH2QP2PGsVsSZzWhC7rmSVFJq79u0tH3IBaImprY4130_provenance
{
dgn-np:NP1366019.RA4WEH2QP2PGsVsSZzWhC7rmSVFJq79u0tH3IBaImprY4130_assertion
dcterms:description
"[The majority of HNPCC families have germline mutations in mismatch repair (MMR) genes, such as MSH2 or MLH1, so that HNPCC cancers characteristically exhibit DNA replication errors (RERs) at microsatellite loci.]. 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:9004127
;
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:NP1366019.RA4WEH2QP2PGsVsSZzWhC7rmSVFJq79u0tH3IBaImprY4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:05+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" .
}