@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP715697.RASMFhF8Q376c0CH6AJw4O5kzHm44jlTDsDabGEkgDn5g
> .
@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:NP715697.RASMFhF8Q376c0CH6AJw4O5kzHm44jlTDsDabGEkgDn5g130_head
{
this:
np:hasAssertion
dgn-np:NP715697.RASMFhF8Q376c0CH6AJw4O5kzHm44jlTDsDabGEkgDn5g130_assertion
;
np:hasProvenance
dgn-np:NP715697.RASMFhF8Q376c0CH6AJw4O5kzHm44jlTDsDabGEkgDn5g130_provenance
;
np:hasPublicationInfo
dgn-np:NP715697.RASMFhF8Q376c0CH6AJw4O5kzHm44jlTDsDabGEkgDn5g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP715697.RASMFhF8Q376c0CH6AJw4O5kzHm44jlTDsDabGEkgDn5g130_assertion
a
np:Assertion
.
dgn-np:NP715697.RASMFhF8Q376c0CH6AJw4O5kzHm44jlTDsDabGEkgDn5g130_provenance
a
np:Provenance
.
dgn-np:NP715697.RASMFhF8Q376c0CH6AJw4O5kzHm44jlTDsDabGEkgDn5g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP715697.RASMFhF8Q376c0CH6AJw4O5kzHm44jlTDsDabGEkgDn5g130_assertion
{
miriam-gene:1982
a
ncit:C16612
.
lld:C0005684
a
ncit:C7057
.
dgn-gda:DGN69783ca2698f71e7ea883d7f67848cfb
sio:SIO_000628
miriam-gene:1982
,
lld:C0005684
;
a
sio:SIO_001121
.
}
dgn-np:NP715697.RASMFhF8Q376c0CH6AJw4O5kzHm44jlTDsDabGEkgDn5g130_provenance
{
dgn-np:NP715697.RASMFhF8Q376c0CH6AJw4O5kzHm44jlTDsDabGEkgDn5g130_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:NP715697.RASMFhF8Q376c0CH6AJw4O5kzHm44jlTDsDabGEkgDn5g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:14+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" .
}