@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP230717.RANe5AkuLlkFbdZY6O-vwWZes_ZUZb85-3MHqB5Eir01Q
> .
@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:NP230717.RANe5AkuLlkFbdZY6O-vwWZes_ZUZb85-3MHqB5Eir01Q130_head
{
this:
np:hasAssertion
dgn-np:NP230717.RANe5AkuLlkFbdZY6O-vwWZes_ZUZb85-3MHqB5Eir01Q130_assertion
;
np:hasProvenance
dgn-np:NP230717.RANe5AkuLlkFbdZY6O-vwWZes_ZUZb85-3MHqB5Eir01Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP230717.RANe5AkuLlkFbdZY6O-vwWZes_ZUZb85-3MHqB5Eir01Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP230717.RANe5AkuLlkFbdZY6O-vwWZes_ZUZb85-3MHqB5Eir01Q130_assertion
a
np:Assertion
.
dgn-np:NP230717.RANe5AkuLlkFbdZY6O-vwWZes_ZUZb85-3MHqB5Eir01Q130_provenance
a
np:Provenance
.
dgn-np:NP230717.RANe5AkuLlkFbdZY6O-vwWZes_ZUZb85-3MHqB5Eir01Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP230717.RANe5AkuLlkFbdZY6O-vwWZes_ZUZb85-3MHqB5Eir01Q130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C1827377
a
ncit:C7057
.
dgn-gda:DGNb72db380e69e13ca73dd3ddbe3de3cef
sio:SIO_000628
miriam-gene:2944
,
lld:C1827377
;
a
sio:SIO_001121
.
}
dgn-np:NP230717.RANe5AkuLlkFbdZY6O-vwWZes_ZUZb85-3MHqB5Eir01Q130_provenance
{
dgn-np:NP230717.RANe5AkuLlkFbdZY6O-vwWZes_ZUZb85-3MHqB5Eir01Q130_assertion
dcterms:description
"[Among the low-penetrant genes, the variants within the genes encoding metabolic enzymes have been consistently associated with susceptibility to bladder cancer and the evidence is compelling for NAT2 slow acetylator and GSTM1 null genotypes.]. 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:21738036
;
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:NP230717.RANe5AkuLlkFbdZY6O-vwWZes_ZUZb85-3MHqB5Eir01Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:09+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" .
}