@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP358395.RATRjmZhLNVswGppTvvlnOMpCgZsvM20m53ACfFAgnSJE
> .
@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/v4.0.0/void/
> .
dgn-np:NP358395.RATRjmZhLNVswGppTvvlnOMpCgZsvM20m53ACfFAgnSJE130_head
{
this:
np:hasAssertion
dgn-np:NP358395.RATRjmZhLNVswGppTvvlnOMpCgZsvM20m53ACfFAgnSJE130_assertion
;
np:hasProvenance
dgn-np:NP358395.RATRjmZhLNVswGppTvvlnOMpCgZsvM20m53ACfFAgnSJE130_provenance
;
np:hasPublicationInfo
dgn-np:NP358395.RATRjmZhLNVswGppTvvlnOMpCgZsvM20m53ACfFAgnSJE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP358395.RATRjmZhLNVswGppTvvlnOMpCgZsvM20m53ACfFAgnSJE130_assertion
a
np:Assertion
.
dgn-np:NP358395.RATRjmZhLNVswGppTvvlnOMpCgZsvM20m53ACfFAgnSJE130_provenance
a
np:Provenance
.
dgn-np:NP358395.RATRjmZhLNVswGppTvvlnOMpCgZsvM20m53ACfFAgnSJE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP358395.RATRjmZhLNVswGppTvvlnOMpCgZsvM20m53ACfFAgnSJE130_assertion
{
miriam-gene:5311
a
ncit:C16612
.
lld:C0085413
a
ncit:C7057
.
dgn-gda:DGN771cd7b00f92ca5d4a73de0d6e63e979
sio:SIO_000628
miriam-gene:5311
,
lld:C0085413
;
a
sio:SIO_001121
.
}
dgn-np:NP358395.RATRjmZhLNVswGppTvvlnOMpCgZsvM20m53ACfFAgnSJE130_provenance
{
dgn-np:NP358395.RATRjmZhLNVswGppTvvlnOMpCgZsvM20m53ACfFAgnSJE130_assertion
dcterms:description
"[The phenotypic variability of autosomal dominant polycystic kidney disease (ADPKD) cannot be explained only by various mutations of two known genes (PKD1 and PKD2), but the influence of other unknown factors should also be considered.]. 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:12077489
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP358395.RATRjmZhLNVswGppTvvlnOMpCgZsvM20m53ACfFAgnSJE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:27+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}