@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP779967.RAN7FYwEgcAQWJZ9EJHHb9K1WqOpAC33N1Dl31PDl3BEo
> .
@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:NP779967.RAN7FYwEgcAQWJZ9EJHHb9K1WqOpAC33N1Dl31PDl3BEo130_head
{
this:
np:hasAssertion
dgn-np:NP779967.RAN7FYwEgcAQWJZ9EJHHb9K1WqOpAC33N1Dl31PDl3BEo130_assertion
;
np:hasProvenance
dgn-np:NP779967.RAN7FYwEgcAQWJZ9EJHHb9K1WqOpAC33N1Dl31PDl3BEo130_provenance
;
np:hasPublicationInfo
dgn-np:NP779967.RAN7FYwEgcAQWJZ9EJHHb9K1WqOpAC33N1Dl31PDl3BEo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP779967.RAN7FYwEgcAQWJZ9EJHHb9K1WqOpAC33N1Dl31PDl3BEo130_assertion
a
np:Assertion
.
dgn-np:NP779967.RAN7FYwEgcAQWJZ9EJHHb9K1WqOpAC33N1Dl31PDl3BEo130_provenance
a
np:Provenance
.
dgn-np:NP779967.RAN7FYwEgcAQWJZ9EJHHb9K1WqOpAC33N1Dl31PDl3BEo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP779967.RAN7FYwEgcAQWJZ9EJHHb9K1WqOpAC33N1Dl31PDl3BEo130_assertion
{
miriam-gene:25865
a
ncit:C16612
.
lld:C0022679
a
ncit:C7057
.
dgn-gda:DGNcba08139f92043d625d6c27300ab11fa
sio:SIO_000628
miriam-gene:25865
,
lld:C0022679
;
a
sio:SIO_001121
.
}
dgn-np:NP779967.RAN7FYwEgcAQWJZ9EJHHb9K1WqOpAC33N1Dl31PDl3BEo130_provenance
{
dgn-np:NP779967.RAN7FYwEgcAQWJZ9EJHHb9K1WqOpAC33N1Dl31PDl3BEo130_assertion
dcterms:description
"[The cloning of PKD1 and PKD2 in recent years has provided the initial steps in defining the mechanisms underlying renal cyst formation in this condition, with the aim of defining pharmacological and genetic interventions that may ameliorate the diverse and often serious clinical manifestations of this disease.]. 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:11212307
;
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:NP779967.RAN7FYwEgcAQWJZ9EJHHb9K1WqOpAC33N1Dl31PDl3BEo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:52+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" .
}