Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP8078.RAW8JmRrxQH-FVF8V1UPyWJIvI_IoB1SM3oRdbviYQpm8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP8078.RAW8JmRrxQH-FVF8V1UPyWJIvI_IoB1SM3oRdbviYQpm8130_assertion type Assertion NP8078.RAW8JmRrxQH-FVF8V1UPyWJIvI_IoB1SM3oRdbviYQpm8130_head.
- NP8078.RAW8JmRrxQH-FVF8V1UPyWJIvI_IoB1SM3oRdbviYQpm8130_assertion description "[A peroxisomal disorder of severe intellectual disability, epilepsy, and cataracts due to fatty acyl-CoA reductase 1 deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8078.RAW8JmRrxQH-FVF8V1UPyWJIvI_IoB1SM3oRdbviYQpm8130_provenance.
- NP8078.RAW8JmRrxQH-FVF8V1UPyWJIvI_IoB1SM3oRdbviYQpm8130_assertion evidence source_evidence_curated NP8078.RAW8JmRrxQH-FVF8V1UPyWJIvI_IoB1SM3oRdbviYQpm8130_provenance.
- NP8078.RAW8JmRrxQH-FVF8V1UPyWJIvI_IoB1SM3oRdbviYQpm8130_assertion SIO_000772 25439727 NP8078.RAW8JmRrxQH-FVF8V1UPyWJIvI_IoB1SM3oRdbviYQpm8130_provenance.
- NP8078.RAW8JmRrxQH-FVF8V1UPyWJIvI_IoB1SM3oRdbviYQpm8130_assertion wasDerivedFrom uniprot-2016 NP8078.RAW8JmRrxQH-FVF8V1UPyWJIvI_IoB1SM3oRdbviYQpm8130_provenance.
- NP8078.RAW8JmRrxQH-FVF8V1UPyWJIvI_IoB1SM3oRdbviYQpm8130_assertion wasGeneratedBy ECO_0000218 NP8078.RAW8JmRrxQH-FVF8V1UPyWJIvI_IoB1SM3oRdbviYQpm8130_provenance.