@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP439485.RAHDI7FT7SHd_jcsZiru85LVpHpTCa_xMBdIMbrccCTl4
> .
@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:NP439485.RAHDI7FT7SHd_jcsZiru85LVpHpTCa_xMBdIMbrccCTl4130_head
{
this:
np:hasAssertion
dgn-np:NP439485.RAHDI7FT7SHd_jcsZiru85LVpHpTCa_xMBdIMbrccCTl4130_assertion
;
np:hasProvenance
dgn-np:NP439485.RAHDI7FT7SHd_jcsZiru85LVpHpTCa_xMBdIMbrccCTl4130_provenance
;
np:hasPublicationInfo
dgn-np:NP439485.RAHDI7FT7SHd_jcsZiru85LVpHpTCa_xMBdIMbrccCTl4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP439485.RAHDI7FT7SHd_jcsZiru85LVpHpTCa_xMBdIMbrccCTl4130_assertion
a
np:Assertion
.
dgn-np:NP439485.RAHDI7FT7SHd_jcsZiru85LVpHpTCa_xMBdIMbrccCTl4130_provenance
a
np:Provenance
.
dgn-np:NP439485.RAHDI7FT7SHd_jcsZiru85LVpHpTCa_xMBdIMbrccCTl4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP439485.RAHDI7FT7SHd_jcsZiru85LVpHpTCa_xMBdIMbrccCTl4130_assertion
{
miriam-gene:5111
a
ncit:C16612
.
lld:C0085548
a
ncit:C7057
.
dgn-gda:DGN015bacb5e3e92aa65e9b7f315f16de00
sio:SIO_000628
miriam-gene:5111
,
lld:C0085548
;
a
sio:SIO_001121
.
}
dgn-np:NP439485.RAHDI7FT7SHd_jcsZiru85LVpHpTCa_xMBdIMbrccCTl4130_provenance
{
dgn-np:NP439485.RAHDI7FT7SHd_jcsZiru85LVpHpTCa_xMBdIMbrccCTl4130_assertion
dcterms:description
"[In this study, which used immunohistochemical methods with an antibody to proliferating cell nuclear antigen (PCNA), the proliferation index (PI) (percentage of PCNA positive cell nuclei among epithelial cells lining the renal cysts) was determined in 10 cases of autosomal dominant polycystic kidney disease (ADPKD), 8 cases of autosomal recessive polycystic kidney disease (ARPKD), and 8 cases of acquired cystic kidney disease (ACKD).]. 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:7703384
;
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:NP439485.RAHDI7FT7SHd_jcsZiru85LVpHpTCa_xMBdIMbrccCTl4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:20+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
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"v2.1.0" .
}