@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP708825.RAR8xeonkje_iAlHrJmAeHkt4LT-V7oHBZBL0mRbqg04E
> .
@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:NP708825.RAR8xeonkje_iAlHrJmAeHkt4LT-V7oHBZBL0mRbqg04E130_head
{
this:
np:hasAssertion
dgn-np:NP708825.RAR8xeonkje_iAlHrJmAeHkt4LT-V7oHBZBL0mRbqg04E130_assertion
;
np:hasProvenance
dgn-np:NP708825.RAR8xeonkje_iAlHrJmAeHkt4LT-V7oHBZBL0mRbqg04E130_provenance
;
np:hasPublicationInfo
dgn-np:NP708825.RAR8xeonkje_iAlHrJmAeHkt4LT-V7oHBZBL0mRbqg04E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP708825.RAR8xeonkje_iAlHrJmAeHkt4LT-V7oHBZBL0mRbqg04E130_assertion
a
np:Assertion
.
dgn-np:NP708825.RAR8xeonkje_iAlHrJmAeHkt4LT-V7oHBZBL0mRbqg04E130_provenance
a
np:Provenance
.
dgn-np:NP708825.RAR8xeonkje_iAlHrJmAeHkt4LT-V7oHBZBL0mRbqg04E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP708825.RAR8xeonkje_iAlHrJmAeHkt4LT-V7oHBZBL0mRbqg04E130_assertion
{
miriam-gene:25865
a
ncit:C16612
.
lld:C0022680
a
ncit:C7057
.
dgn-gda:DGN3766304be6e18327c0f4b34c538499c7
sio:SIO_000628
miriam-gene:25865
,
lld:C0022680
;
a
sio:SIO_001121
.
}
dgn-np:NP708825.RAR8xeonkje_iAlHrJmAeHkt4LT-V7oHBZBL0mRbqg04E130_provenance
{
dgn-np:NP708825.RAR8xeonkje_iAlHrJmAeHkt4LT-V7oHBZBL0mRbqg04E130_assertion
dcterms:description
"[An initiative of the Polycystic Kidney Disease Foundation, PKDB is a publicly accessible database that aims to streamline the evaluation of PKD1 and PKD2 gene variants detected in samples from those with ADPKD, as well as to assist ongoing clinical and molecular research in the field.]. 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:17370309
;
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:NP708825.RAR8xeonkje_iAlHrJmAeHkt4LT-V7oHBZBL0mRbqg04E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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" .
}