Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3837.RAUNJVu5kT-61H_A1kLJOYUMhRFJ5pf2pPKK28pVUOUZk130_assertion> ?p ?o ?g. }
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- NP3837.RAUNJVu5kT-61H_A1kLJOYUMhRFJ5pf2pPKK28pVUOUZk130_assertion type Assertion NP3837.RAUNJVu5kT-61H_A1kLJOYUMhRFJ5pf2pPKK28pVUOUZk130_head.
- NP3837.RAUNJVu5kT-61H_A1kLJOYUMhRFJ5pf2pPKK28pVUOUZk130_assertion wasGeneratedBy ECO_0000218 NP3837.RAUNJVu5kT-61H_A1kLJOYUMhRFJ5pf2pPKK28pVUOUZk130_provenance.
- NP3837.RAUNJVu5kT-61H_A1kLJOYUMhRFJ5pf2pPKK28pVUOUZk130_assertion wasDerivedFrom uniprot-20130724 NP3837.RAUNJVu5kT-61H_A1kLJOYUMhRFJ5pf2pPKK28pVUOUZk130_provenance.
- NP3837.RAUNJVu5kT-61H_A1kLJOYUMhRFJ5pf2pPKK28pVUOUZk130_assertion SIO_000772 12927431 NP3837.RAUNJVu5kT-61H_A1kLJOYUMhRFJ5pf2pPKK28pVUOUZk130_provenance.
- NP3837.RAUNJVu5kT-61H_A1kLJOYUMhRFJ5pf2pPKK28pVUOUZk130_assertion evidence source_evidence_curated NP3837.RAUNJVu5kT-61H_A1kLJOYUMhRFJ5pf2pPKK28pVUOUZk130_provenance.
- NP3837.RAUNJVu5kT-61H_A1kLJOYUMhRFJ5pf2pPKK28pVUOUZk130_assertion description "[LMNA mutations in atypical Werner's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3837.RAUNJVu5kT-61H_A1kLJOYUMhRFJ5pf2pPKK28pVUOUZk130_provenance.