@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP129453.RAd2BwLUh7PRud6BGVAXn9y6Tn14G9tIGB0Ds4U-JBWNs
> .
@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:NP129453.RAd2BwLUh7PRud6BGVAXn9y6Tn14G9tIGB0Ds4U-JBWNs130_head
{
this:
np:hasAssertion
dgn-np:NP129453.RAd2BwLUh7PRud6BGVAXn9y6Tn14G9tIGB0Ds4U-JBWNs130_assertion
;
np:hasProvenance
dgn-np:NP129453.RAd2BwLUh7PRud6BGVAXn9y6Tn14G9tIGB0Ds4U-JBWNs130_provenance
;
np:hasPublicationInfo
dgn-np:NP129453.RAd2BwLUh7PRud6BGVAXn9y6Tn14G9tIGB0Ds4U-JBWNs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP129453.RAd2BwLUh7PRud6BGVAXn9y6Tn14G9tIGB0Ds4U-JBWNs130_assertion
a
np:Assertion
.
dgn-np:NP129453.RAd2BwLUh7PRud6BGVAXn9y6Tn14G9tIGB0Ds4U-JBWNs130_provenance
a
np:Provenance
.
dgn-np:NP129453.RAd2BwLUh7PRud6BGVAXn9y6Tn14G9tIGB0Ds4U-JBWNs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP129453.RAd2BwLUh7PRud6BGVAXn9y6Tn14G9tIGB0Ds4U-JBWNs130_assertion
{
miriam-gene:7520
a
ncit:C16612
.
lld:C0005695
a
ncit:C7057
.
dgn-gda:DGN8c70e4c300883a8fa45fb971e69bd556
sio:SIO_000628
miriam-gene:7520
,
lld:C0005695
;
a
sio:SIO_001122
.
}
dgn-np:NP129453.RAd2BwLUh7PRud6BGVAXn9y6Tn14G9tIGB0Ds4U-JBWNs130_provenance
{
dgn-np:NP129453.RAd2BwLUh7PRud6BGVAXn9y6Tn14G9tIGB0Ds4U-JBWNs130_assertion
dcterms:description
"[Although the different genotypes were not associated with the risk of bladder cancer, individuals not carrying the two tandem repeats allele had an increased risk of bladder cancer compared with those carrying the allele with two repeats.]. 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:17904587
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP129453.RAd2BwLUh7PRud6BGVAXn9y6Tn14G9tIGB0Ds4U-JBWNs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:07+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" .
}