@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP626877.RAYwWS70TY84xzaB_DOi57cafRkRp0Xykvbzx9qK9eJCM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP626877.RAYwWS70TY84xzaB_DOi57cafRkRp0Xykvbzx9qK9eJCM130_head
{
this:
np:hasAssertion
dgn-np:NP626877.RAYwWS70TY84xzaB_DOi57cafRkRp0Xykvbzx9qK9eJCM130_assertion
;
np:hasProvenance
dgn-np:NP626877.RAYwWS70TY84xzaB_DOi57cafRkRp0Xykvbzx9qK9eJCM130_provenance
;
np:hasPublicationInfo
dgn-np:NP626877.RAYwWS70TY84xzaB_DOi57cafRkRp0Xykvbzx9qK9eJCM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP626877.RAYwWS70TY84xzaB_DOi57cafRkRp0Xykvbzx9qK9eJCM130_assertion
a
np:Assertion
.
dgn-np:NP626877.RAYwWS70TY84xzaB_DOi57cafRkRp0Xykvbzx9qK9eJCM130_provenance
a
np:Provenance
.
dgn-np:NP626877.RAYwWS70TY84xzaB_DOi57cafRkRp0Xykvbzx9qK9eJCM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP626877.RAYwWS70TY84xzaB_DOi57cafRkRp0Xykvbzx9qK9eJCM130_assertion
{
miriam-gene:5311
a
ncit:C16612
.
lld:C0010709
a
ncit:C7057
.
dgn-gda:DGN2fa10a52b3343906b21f241a4b0ee360
sio:SIO_000628
miriam-gene:5311
,
lld:C0010709
;
a
sio:SIO_001121
.
}
dgn-np:NP626877.RAYwWS70TY84xzaB_DOi57cafRkRp0Xykvbzx9qK9eJCM130_provenance
{
dgn-np:NP626877.RAYwWS70TY84xzaB_DOi57cafRkRp0Xykvbzx9qK9eJCM130_assertion
dcterms:description
"[The spectrum of germ-line mutations in both genes and the somatic mutations identified from individual PKD1 or PKD2 cysts indicate that loss of function of either PKD1 or PKD2 is the mechanism of cystogenesis in autosomal-dominant polycystic kidney 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:11195048
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP626877.RAYwWS70TY84xzaB_DOi57cafRkRp0Xykvbzx9qK9eJCM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:55+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}