SPARQL
Query
Update
Search
Quick
Advanced
Co-occurrence
RelFinder
About
Sources
Admin
System Info
Repository Management
Search Configuration
Sources
Renal dysfunction
Source:
http://linkedlifedata.com/resource/phenotype/id/HP:0000082
Search
Subject
Predicate
Object
All
(
19
)
Download in:
JSON
RDF
N3/Turtle
N-Triples
Named Graph
All
UniProt
NCBIGene
DrugBank
ClinicalTrials
UMLS
PubMed
Mappings
MentionedEntities
Language
All
English
Español
Português
Français
Deutsch
Русский
日本語
Български
Inference
Explicit and implicit
Explicit only
Implicit only
Statements in which the resource exists.
Subject
Predicate
Object
Context
phenotype:HP:0000082
rdf:type
skos:Concept
lld:phenotype
phenotype:HP:0000082
skos:definition
"An `abnormal` (PATO:0000460) `functionality` (PATO:0001509) of the `kidney` (FMA:7203)." [HPO:probinson]
lld:phenotype
phenotype:HP:0000082
skos:inScheme
lld:phenotype
lld:phenotype
phenotype:HP:0000082
skos:prefLabel
Abnormality of renal physiology
lld:phenotype
phenotype:HP:0000082
skos:altLabel
Renal dysfunction
lld:phenotype
phenotype:HP:0000082
skos:altLabel
Impaired renal function
lld:phenotype
phenotype:HP:0000082
skos:altLabel
Decreased renal function
lld:phenotype
phenotype:HP:0000082
skos:altLabel
Loss of renal function
lld:phenotype
phenotype:HP:0000082
skos:altLabel
Reduced renal function
lld:phenotype
phenotype:HP:0000082
skos:altLabel
Renal functional abnormality
lld:phenotype
phenotype:HP:0000082
skos:notation
UMLS:C1848822 "Renal dysfunction"
lld:phenotype
phenotype:HP:0000082
skos:broader
phenotype:HP:0011277
lld:phenotype
phenotype:HP:0000083
skos:broader
phenotype:HP:0000082
lld:phenotype
phenotype:HP:0000100
skos:broader
phenotype:HP:0000082
lld:phenotype
phenotype:HP:0011036
skos:broader
phenotype:HP:0000082
lld:phenotype
phenotype:HP:0000127
skos:broader
phenotype:HP:0000082
lld:phenotype
phenotype:HP:0000124
skos:broader
phenotype:HP:0000082
lld:phenotype
phenotype:HP:0011038
skos:broader
phenotype:HP:0000082
lld:phenotype
phenotype:HP:0100515
skos:broader
phenotype:HP:0000082
lld:phenotype