Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1336132.RALSDY2AFlClW3LmfrmvzpKInOHFXa1vW53oJEGcq10cY130_assertion> ?p ?o ?g. }
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- NP1336132.RALSDY2AFlClW3LmfrmvzpKInOHFXa1vW53oJEGcq10cY130_assertion type Assertion NP1336132.RALSDY2AFlClW3LmfrmvzpKInOHFXa1vW53oJEGcq10cY130_head.
- NP1336132.RALSDY2AFlClW3LmfrmvzpKInOHFXa1vW53oJEGcq10cY130_assertion wasGeneratedBy ECO_0000203 NP1336132.RALSDY2AFlClW3LmfrmvzpKInOHFXa1vW53oJEGcq10cY130_provenance.
- NP1336132.RALSDY2AFlClW3LmfrmvzpKInOHFXa1vW53oJEGcq10cY130_assertion wasDerivedFrom befree-2016 NP1336132.RALSDY2AFlClW3LmfrmvzpKInOHFXa1vW53oJEGcq10cY130_provenance.
- NP1336132.RALSDY2AFlClW3LmfrmvzpKInOHFXa1vW53oJEGcq10cY130_assertion SIO_000772 8225311 NP1336132.RALSDY2AFlClW3LmfrmvzpKInOHFXa1vW53oJEGcq10cY130_provenance.
- NP1336132.RALSDY2AFlClW3LmfrmvzpKInOHFXa1vW53oJEGcq10cY130_assertion evidence source_evidence_literature NP1336132.RALSDY2AFlClW3LmfrmvzpKInOHFXa1vW53oJEGcq10cY130_provenance.
- NP1336132.RALSDY2AFlClW3LmfrmvzpKInOHFXa1vW53oJEGcq10cY130_assertion description "[Deletion of arginine (608) in acid sphingomyelinase is the prevalent mutation among Niemann-Pick disease type B patients from northern Africa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1336132.RALSDY2AFlClW3LmfrmvzpKInOHFXa1vW53oJEGcq10cY130_provenance.