Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP301.RATFwmEBJ81FcfzBr081PvHMmfG6gZzeejqA-eyOd9kiE130_assertion> ?p ?o ?g. }
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- NP301.RATFwmEBJ81FcfzBr081PvHMmfG6gZzeejqA-eyOd9kiE130_assertion type Assertion NP301.RATFwmEBJ81FcfzBr081PvHMmfG6gZzeejqA-eyOd9kiE130_head.
- NP301.RATFwmEBJ81FcfzBr081PvHMmfG6gZzeejqA-eyOd9kiE130_assertion wasGeneratedBy ECO_0000218 NP301.RATFwmEBJ81FcfzBr081PvHMmfG6gZzeejqA-eyOd9kiE130_provenance.
- NP301.RATFwmEBJ81FcfzBr081PvHMmfG6gZzeejqA-eyOd9kiE130_assertion wasDerivedFrom uniprot-20150221 NP301.RATFwmEBJ81FcfzBr081PvHMmfG6gZzeejqA-eyOd9kiE130_provenance.
- NP301.RATFwmEBJ81FcfzBr081PvHMmfG6gZzeejqA-eyOd9kiE130_assertion SIO_000772 11956200 NP301.RATFwmEBJ81FcfzBr081PvHMmfG6gZzeejqA-eyOd9kiE130_provenance.
- NP301.RATFwmEBJ81FcfzBr081PvHMmfG6gZzeejqA-eyOd9kiE130_assertion evidence source_evidence_curated NP301.RATFwmEBJ81FcfzBr081PvHMmfG6gZzeejqA-eyOd9kiE130_provenance.
- NP301.RATFwmEBJ81FcfzBr081PvHMmfG6gZzeejqA-eyOd9kiE130_assertion description "[Thus, an assembly defect of DDP1 is the molecular basis of Mohr-Tranebjaerg syndrome in patients carrying the C66W mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP301.RATFwmEBJ81FcfzBr081PvHMmfG6gZzeejqA-eyOd9kiE130_provenance.