Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP938258.RAc6vzgvgmYBTx5GzjGDa4EUI4hNwCtig1g_T-3nmL2uc130_assertion> ?p ?o ?g. }
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- NP938258.RAc6vzgvgmYBTx5GzjGDa4EUI4hNwCtig1g_T-3nmL2uc130_assertion type Assertion NP938258.RAc6vzgvgmYBTx5GzjGDa4EUI4hNwCtig1g_T-3nmL2uc130_head.
- NP938258.RAc6vzgvgmYBTx5GzjGDa4EUI4hNwCtig1g_T-3nmL2uc130_assertion description "[The presence of VCP mutations in patients with sporadic ALS, sporadic ALS-FTD, and progressive muscular atrophy (PMA), a known clinical mimic of inclusion body myopathy, is not known.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP938258.RAc6vzgvgmYBTx5GzjGDa4EUI4hNwCtig1g_T-3nmL2uc130_provenance.
- NP938258.RAc6vzgvgmYBTx5GzjGDa4EUI4hNwCtig1g_T-3nmL2uc130_assertion evidence source_evidence_literature NP938258.RAc6vzgvgmYBTx5GzjGDa4EUI4hNwCtig1g_T-3nmL2uc130_provenance.
- NP938258.RAc6vzgvgmYBTx5GzjGDa4EUI4hNwCtig1g_T-3nmL2uc130_assertion SIO_000772 22078486 NP938258.RAc6vzgvgmYBTx5GzjGDa4EUI4hNwCtig1g_T-3nmL2uc130_provenance.
- NP938258.RAc6vzgvgmYBTx5GzjGDa4EUI4hNwCtig1g_T-3nmL2uc130_assertion wasDerivedFrom befree-2016 NP938258.RAc6vzgvgmYBTx5GzjGDa4EUI4hNwCtig1g_T-3nmL2uc130_provenance.
- NP938258.RAc6vzgvgmYBTx5GzjGDa4EUI4hNwCtig1g_T-3nmL2uc130_assertion wasGeneratedBy ECO_0000203 NP938258.RAc6vzgvgmYBTx5GzjGDa4EUI4hNwCtig1g_T-3nmL2uc130_provenance.