@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP573122.RAzkjD6zHOXhHAAVO82YO8jn9SSTXBMWMHE2yyt7i930c
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP573122.RAzkjD6zHOXhHAAVO82YO8jn9SSTXBMWMHE2yyt7i930c130_head
{
this:
np:hasAssertion
dgn-np:NP573122.RAzkjD6zHOXhHAAVO82YO8jn9SSTXBMWMHE2yyt7i930c130_assertion
;
np:hasProvenance
dgn-np:NP573122.RAzkjD6zHOXhHAAVO82YO8jn9SSTXBMWMHE2yyt7i930c130_provenance
;
np:hasPublicationInfo
dgn-np:NP573122.RAzkjD6zHOXhHAAVO82YO8jn9SSTXBMWMHE2yyt7i930c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP573122.RAzkjD6zHOXhHAAVO82YO8jn9SSTXBMWMHE2yyt7i930c130_assertion
a
np:Assertion
.
dgn-np:NP573122.RAzkjD6zHOXhHAAVO82YO8jn9SSTXBMWMHE2yyt7i930c130_provenance
a
np:Provenance
.
dgn-np:NP573122.RAzkjD6zHOXhHAAVO82YO8jn9SSTXBMWMHE2yyt7i930c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP573122.RAzkjD6zHOXhHAAVO82YO8jn9SSTXBMWMHE2yyt7i930c130_assertion
{
miriam-gene:5378
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGNfbcd95f042d1eeabf02a1239260846ea
sio:SIO_000628
miriam-gene:5378
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP573122.RAzkjD6zHOXhHAAVO82YO8jn9SSTXBMWMHE2yyt7i930c130_provenance
{
dgn-np:NP573122.RAzkjD6zHOXhHAAVO82YO8jn9SSTXBMWMHE2yyt7i930c130_assertion
dcterms:description
"[Mutations affecting human mismatch repair (MMR) genes (MLH1, MSH2, PMS1, PMS2, and MSH6) cause tumour predisposition in hereditary nonpolyposis colorectal cancer (HNPCC) syndrome, and an association has been demonstrated with the replication error (RER) phenotype in most colorectal and some extracolonic neoplasms.]. 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:10448273
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP573122.RAzkjD6zHOXhHAAVO82YO8jn9SSTXBMWMHE2yyt7i930c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:45+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}