@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP526569.RAD88Zgd2TialzPHtoCV_uftSHggwLRzUKWMRiptQkmnQ
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP526569.RAD88Zgd2TialzPHtoCV_uftSHggwLRzUKWMRiptQkmnQ130_assertion
;
np:hasProvenance
dgn-np:NP526569.RAD88Zgd2TialzPHtoCV_uftSHggwLRzUKWMRiptQkmnQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP526569.RAD88Zgd2TialzPHtoCV_uftSHggwLRzUKWMRiptQkmnQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP526569.RAD88Zgd2TialzPHtoCV_uftSHggwLRzUKWMRiptQkmnQ130_assertion
a
np:Assertion
.
dgn-np:NP526569.RAD88Zgd2TialzPHtoCV_uftSHggwLRzUKWMRiptQkmnQ130_provenance
a
np:Provenance
.
dgn-np:NP526569.RAD88Zgd2TialzPHtoCV_uftSHggwLRzUKWMRiptQkmnQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP526569.RAD88Zgd2TialzPHtoCV_uftSHggwLRzUKWMRiptQkmnQ130_assertion
{
miriam-gene:252969
a
ncit:C16612
.
lld:C1302401
a
ncit:C7057
.
dgn-gda:DGN117a0efdc597ee1c6fa74980895bac14
sio:SIO_000628
miriam-gene:252969
,
lld:C1302401
;
a
sio:SIO_001121
.
}
dgn-np:NP526569.RAD88Zgd2TialzPHtoCV_uftSHggwLRzUKWMRiptQkmnQ130_provenance
{
dgn-np:NP526569.RAD88Zgd2TialzPHtoCV_uftSHggwLRzUKWMRiptQkmnQ130_assertion
dcterms:description
"[To assess the contribution of inherited variants in genes involved in base excision repair and oxidative DNA damage including MUTYH, OGG1, NEIL1, NEIL2, NEIL3, NUDT1 and NTH1 to the multiple colorectal adenoma phenotype.]. 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:18515411
;
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:NP526569.RAD88Zgd2TialzPHtoCV_uftSHggwLRzUKWMRiptQkmnQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:15+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" .
}