@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP805131.RAxpGbsbjOcIMQdsw9w1VNTP0HKTcJHngKxe0OPThzYiA
> .
@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:NP805131.RAxpGbsbjOcIMQdsw9w1VNTP0HKTcJHngKxe0OPThzYiA130_head
{
this:
np:hasAssertion
dgn-np:NP805131.RAxpGbsbjOcIMQdsw9w1VNTP0HKTcJHngKxe0OPThzYiA130_assertion
;
np:hasProvenance
dgn-np:NP805131.RAxpGbsbjOcIMQdsw9w1VNTP0HKTcJHngKxe0OPThzYiA130_provenance
;
np:hasPublicationInfo
dgn-np:NP805131.RAxpGbsbjOcIMQdsw9w1VNTP0HKTcJHngKxe0OPThzYiA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP805131.RAxpGbsbjOcIMQdsw9w1VNTP0HKTcJHngKxe0OPThzYiA130_assertion
a
np:Assertion
.
dgn-np:NP805131.RAxpGbsbjOcIMQdsw9w1VNTP0HKTcJHngKxe0OPThzYiA130_provenance
a
np:Provenance
.
dgn-np:NP805131.RAxpGbsbjOcIMQdsw9w1VNTP0HKTcJHngKxe0OPThzYiA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP805131.RAxpGbsbjOcIMQdsw9w1VNTP0HKTcJHngKxe0OPThzYiA130_assertion
{
miriam-gene:9
a
ncit:C16612
.
lld:C0699885
a
ncit:C7057
.
dgn-gda:DGN0b3638628153e363dfcefde748f34b82
sio:SIO_000628
miriam-gene:9
,
lld:C0699885
;
a
sio:SIO_001121
.
}
dgn-np:NP805131.RAxpGbsbjOcIMQdsw9w1VNTP0HKTcJHngKxe0OPThzYiA130_provenance
{
dgn-np:NP805131.RAxpGbsbjOcIMQdsw9w1VNTP0HKTcJHngKxe0OPThzYiA130_assertion
dcterms:description
"[In collaborative studies, we now have found that NAT1 is also expressed polymorphically in human bladder due to mutations in the NAT1 polyadenylation signal, which has recently been associated with increased bladder cancer risk.]. 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:8597119
;
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:NP805131.RAxpGbsbjOcIMQdsw9w1VNTP0HKTcJHngKxe0OPThzYiA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:14+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" .
}