@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP291646.RANwmoyC-Q-M5m3GO-OXj8YxPlzh0P3vuY41hMW_DzYQM
> .
@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:NP291646.RANwmoyC-Q-M5m3GO-OXj8YxPlzh0P3vuY41hMW_DzYQM130_head
{
this:
np:hasAssertion
dgn-np:NP291646.RANwmoyC-Q-M5m3GO-OXj8YxPlzh0P3vuY41hMW_DzYQM130_assertion
;
np:hasProvenance
dgn-np:NP291646.RANwmoyC-Q-M5m3GO-OXj8YxPlzh0P3vuY41hMW_DzYQM130_provenance
;
np:hasPublicationInfo
dgn-np:NP291646.RANwmoyC-Q-M5m3GO-OXj8YxPlzh0P3vuY41hMW_DzYQM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP291646.RANwmoyC-Q-M5m3GO-OXj8YxPlzh0P3vuY41hMW_DzYQM130_assertion
a
np:Assertion
.
dgn-np:NP291646.RANwmoyC-Q-M5m3GO-OXj8YxPlzh0P3vuY41hMW_DzYQM130_provenance
a
np:Provenance
.
dgn-np:NP291646.RANwmoyC-Q-M5m3GO-OXj8YxPlzh0P3vuY41hMW_DzYQM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP291646.RANwmoyC-Q-M5m3GO-OXj8YxPlzh0P3vuY41hMW_DzYQM130_assertion
{
miriam-gene:5310
a
ncit:C16612
.
lld:C0010709
a
ncit:C7057
.
dgn-gda:DGNfcd9be35b089c4182ce592d0077b793e
sio:SIO_000628
miriam-gene:5310
,
lld:C0010709
;
a
sio:SIO_001121
.
}
dgn-np:NP291646.RANwmoyC-Q-M5m3GO-OXj8YxPlzh0P3vuY41hMW_DzYQM130_provenance
{
dgn-np:NP291646.RANwmoyC-Q-M5m3GO-OXj8YxPlzh0P3vuY41hMW_DzYQM130_assertion
dcterms:description
"[In the former disease the diagnostic utility of renal ultrasound was determined, as was the prognostic impact of genotype, the role of the renin-angiotensin system in the pre-hypertensive phase, the potential for somatic mutations of the PKD2 gene, or the combination of mutations in the PKD1 and PKD2 genes, in single cells to induce cysts, and the demonstration that human transheterozygotes of PKD1 and -2 are not embryonically lethal.]. 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:12028433
;
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:NP291646.RANwmoyC-Q-M5m3GO-OXj8YxPlzh0P3vuY41hMW_DzYQM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:46+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" .
}