@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg
> .
@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:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_head
{
this:
np:hasAssertion
dgn-np:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_assertion
;
np:hasProvenance
dgn-np:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_provenance
;
np:hasPublicationInfo
dgn-np:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_assertion
a
np:Assertion
.
dgn-np:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_provenance
a
np:Provenance
.
dgn-np:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN0beca3edad023b594e10ce2af6254db5
sio:SIO_000628
miriam-gene:4292
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_provenance
{
dgn-np:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_assertion
dcterms:description
"[Germline mutations or the malfunctioning of postreplicative mismatch repair genes (MMR) are responsible of hereditary nonpolyposis colorectal cancer (HNPCC), and are also implied in some sporadic colorectal cancer (CRC) forms without any familial history of this disease.]. 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:19665066
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}