@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP905254.RAiV-9AiK1cIzwTjRAfd0kZ7dWTfZgDkdmGkGrrP6vJP8
> .
@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:NP905254.RAiV-9AiK1cIzwTjRAfd0kZ7dWTfZgDkdmGkGrrP6vJP8130_head
{
this:
np:hasAssertion
dgn-np:NP905254.RAiV-9AiK1cIzwTjRAfd0kZ7dWTfZgDkdmGkGrrP6vJP8130_assertion
;
np:hasProvenance
dgn-np:NP905254.RAiV-9AiK1cIzwTjRAfd0kZ7dWTfZgDkdmGkGrrP6vJP8130_provenance
;
np:hasPublicationInfo
dgn-np:NP905254.RAiV-9AiK1cIzwTjRAfd0kZ7dWTfZgDkdmGkGrrP6vJP8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP905254.RAiV-9AiK1cIzwTjRAfd0kZ7dWTfZgDkdmGkGrrP6vJP8130_assertion
a
np:Assertion
.
dgn-np:NP905254.RAiV-9AiK1cIzwTjRAfd0kZ7dWTfZgDkdmGkGrrP6vJP8130_provenance
a
np:Provenance
.
dgn-np:NP905254.RAiV-9AiK1cIzwTjRAfd0kZ7dWTfZgDkdmGkGrrP6vJP8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP905254.RAiV-9AiK1cIzwTjRAfd0kZ7dWTfZgDkdmGkGrrP6vJP8130_assertion
{
miriam-gene:4521
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN9feeab7c622deeaca5e02f0d10151b19
sio:SIO_000628
miriam-gene:4521
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP905254.RAiV-9AiK1cIzwTjRAfd0kZ7dWTfZgDkdmGkGrrP6vJP8130_provenance
{
dgn-np:NP905254.RAiV-9AiK1cIzwTjRAfd0kZ7dWTfZgDkdmGkGrrP6vJP8130_assertion
dcterms:description
"[The hMYH and NEIL1 gene loci in addition to the DNA repair genes hOGG1, NTHL1 and NUDT1 were analyzed in 66 PSC patients (37 with CCA and 29 without cancer) by complete genomic sequencing of exons and adjacent intronic regions.]. 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:19443904
;
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:NP905254.RAiV-9AiK1cIzwTjRAfd0kZ7dWTfZgDkdmGkGrrP6vJP8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:16+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" .
}