Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP37880.RABPDpDwOiztfE2WhKtsPxYxAEAYpE4UlgVPTxO9sXUo4130_assertion> ?p ?o ?g. }
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- NP37880.RABPDpDwOiztfE2WhKtsPxYxAEAYpE4UlgVPTxO9sXUo4130_assertion type Assertion NP37880.RABPDpDwOiztfE2WhKtsPxYxAEAYpE4UlgVPTxO9sXUo4130_head.
- NP37880.RABPDpDwOiztfE2WhKtsPxYxAEAYpE4UlgVPTxO9sXUo4130_assertion wasGeneratedBy ECO_0000218 NP37880.RABPDpDwOiztfE2WhKtsPxYxAEAYpE4UlgVPTxO9sXUo4130_provenance.
- NP37880.RABPDpDwOiztfE2WhKtsPxYxAEAYpE4UlgVPTxO9sXUo4130_assertion wasDerivedFrom ctd_human-2016 NP37880.RABPDpDwOiztfE2WhKtsPxYxAEAYpE4UlgVPTxO9sXUo4130_provenance.
- NP37880.RABPDpDwOiztfE2WhKtsPxYxAEAYpE4UlgVPTxO9sXUo4130_assertion SIO_000772 9657769 NP37880.RABPDpDwOiztfE2WhKtsPxYxAEAYpE4UlgVPTxO9sXUo4130_provenance.
- NP37880.RABPDpDwOiztfE2WhKtsPxYxAEAYpE4UlgVPTxO9sXUo4130_assertion evidence source_evidence_curated NP37880.RABPDpDwOiztfE2WhKtsPxYxAEAYpE4UlgVPTxO9sXUo4130_provenance.
- NP37880.RABPDpDwOiztfE2WhKtsPxYxAEAYpE4UlgVPTxO9sXUo4130_assertion description "[Rhnull disease: the amorph type results from a novel double mutation in RhCe gene on D-negative background.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP37880.RABPDpDwOiztfE2WhKtsPxYxAEAYpE4UlgVPTxO9sXUo4130_provenance.