Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1336132.RALSDY2AFlClW3LmfrmvzpKInOHFXa1vW53oJEGcq10cY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1336132.RALSDY2AFlClW3LmfrmvzpKInOHFXa1vW53oJEGcq10cY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1336132.RALSDY2AFlClW3LmfrmvzpKInOHFXa1vW53oJEGcq10cY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1336132.RALSDY2AFlClW3LmfrmvzpKInOHFXa1vW53oJEGcq10cY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1336132.RALSDY2AFlClW3LmfrmvzpKInOHFXa1vW53oJEGcq10cY130_provenance.
- 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.