@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP503486.RAOULoLBD0j-Hs97N2TUHi8yejalAuCH_EcunpAzQ3yTM
> .
@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:NP503486.RAOULoLBD0j-Hs97N2TUHi8yejalAuCH_EcunpAzQ3yTM130_head
{
this:
np:hasAssertion
dgn-np:NP503486.RAOULoLBD0j-Hs97N2TUHi8yejalAuCH_EcunpAzQ3yTM130_assertion
;
np:hasProvenance
dgn-np:NP503486.RAOULoLBD0j-Hs97N2TUHi8yejalAuCH_EcunpAzQ3yTM130_provenance
;
np:hasPublicationInfo
dgn-np:NP503486.RAOULoLBD0j-Hs97N2TUHi8yejalAuCH_EcunpAzQ3yTM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP503486.RAOULoLBD0j-Hs97N2TUHi8yejalAuCH_EcunpAzQ3yTM130_assertion
a
np:Assertion
.
dgn-np:NP503486.RAOULoLBD0j-Hs97N2TUHi8yejalAuCH_EcunpAzQ3yTM130_provenance
a
np:Provenance
.
dgn-np:NP503486.RAOULoLBD0j-Hs97N2TUHi8yejalAuCH_EcunpAzQ3yTM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP503486.RAOULoLBD0j-Hs97N2TUHi8yejalAuCH_EcunpAzQ3yTM130_assertion
{
miriam-gene:5308
a
ncit:C16612
.
lld:C0005684
a
ncit:C7057
.
dgn-gda:DGNe10647b81ef4e4320d291542a86580ff
sio:SIO_000628
miriam-gene:5308
,
lld:C0005684
;
a
sio:SIO_001121
.
}
dgn-np:NP503486.RAOULoLBD0j-Hs97N2TUHi8yejalAuCH_EcunpAzQ3yTM130_provenance
{
dgn-np:NP503486.RAOULoLBD0j-Hs97N2TUHi8yejalAuCH_EcunpAzQ3yTM130_assertion
dcterms:description
"[Genetic variations in the RGS pathway were associated with the overall risk of bladder cancer, recurrence, and progression in patients with NMIBC and with the risk of death in patients with MIBC.]. 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:23529717
;
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:NP503486.RAOULoLBD0j-Hs97N2TUHi8yejalAuCH_EcunpAzQ3yTM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:00+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" .
}