@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM
> .
@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:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_head
{
this:
np:hasAssertion
dgn-np:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_assertion
;
np:hasProvenance
dgn-np:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_provenance
;
np:hasPublicationInfo
dgn-np:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_assertion
a
np:Assertion
.
dgn-np:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_provenance
a
np:Provenance
.
dgn-np:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_assertion
{
miriam-gene:5587
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN1d4d4a99a42abfb3cac811c01a264571
sio:SIO_000628
miriam-gene:5587
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_provenance
{
dgn-np:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_assertion
dcterms:description
"[Our clinical analysis, yet based only on a limited number of PKD2 subjects, does not definitely support the concept of a milder phenotype and prognosis in PKD2 versus PKD1 patients, in terms of mean age of diagnosis (29 vs. 29 years), mean age at onset of arterial hypertension (33 vs. 33 years), more favourable renal function or ultrasound findings.]. 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:9595261
;
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:NP767336.RAWGhNrYw9P845_MLc6xKL7AGRayDAnB20KbYtmctvwSM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:44+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" .
}