@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0
> .
@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:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_head
{
this:
np:hasAssertion
dgn-np:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_assertion
;
np:hasProvenance
dgn-np:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_provenance
;
np:hasPublicationInfo
dgn-np:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_assertion
a
np:Assertion
.
dgn-np:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_provenance
a
np:Provenance
.
dgn-np:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGNc13f82f371b63ef8b098c9f0cc483c74
sio:SIO_000628
miriam-gene:4436
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_provenance
{
dgn-np:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_assertion
dcterms:description
"[A substantial proportion of MLH1 and MSH2 gene mutations in hereditary nonpolyposis colon cancer syndrome (HNPCC) families are characterized by nucleotide substitutions, either within the coding sequence (missense or silent mutations) or in introns.]. 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:16395668
;
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:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:44+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" .
}