Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP840216.RAedaHJnrCNJ8i0-ShmBy8VorcrXRiLgwcf8t4lTLP9Fs130_assertion> ?p ?o ?g. }
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- NP840216.RAedaHJnrCNJ8i0-ShmBy8VorcrXRiLgwcf8t4lTLP9Fs130_assertion type Assertion NP840216.RAedaHJnrCNJ8i0-ShmBy8VorcrXRiLgwcf8t4lTLP9Fs130_head.
- NP840216.RAedaHJnrCNJ8i0-ShmBy8VorcrXRiLgwcf8t4lTLP9Fs130_assertion description "[Mutations in UBQLN2 and SIGMAR1 genes are rare in Korean patients with amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP840216.RAedaHJnrCNJ8i0-ShmBy8VorcrXRiLgwcf8t4lTLP9Fs130_provenance.
- NP840216.RAedaHJnrCNJ8i0-ShmBy8VorcrXRiLgwcf8t4lTLP9Fs130_assertion evidence source_evidence_literature NP840216.RAedaHJnrCNJ8i0-ShmBy8VorcrXRiLgwcf8t4lTLP9Fs130_provenance.
- NP840216.RAedaHJnrCNJ8i0-ShmBy8VorcrXRiLgwcf8t4lTLP9Fs130_assertion SIO_000772 24684794 NP840216.RAedaHJnrCNJ8i0-ShmBy8VorcrXRiLgwcf8t4lTLP9Fs130_provenance.
- NP840216.RAedaHJnrCNJ8i0-ShmBy8VorcrXRiLgwcf8t4lTLP9Fs130_assertion wasDerivedFrom befree-20150227 NP840216.RAedaHJnrCNJ8i0-ShmBy8VorcrXRiLgwcf8t4lTLP9Fs130_provenance.
- NP840216.RAedaHJnrCNJ8i0-ShmBy8VorcrXRiLgwcf8t4lTLP9Fs130_assertion wasGeneratedBy ECO_0000203 NP840216.RAedaHJnrCNJ8i0-ShmBy8VorcrXRiLgwcf8t4lTLP9Fs130_provenance.