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- source_evidence_literature type ECO_0000212 NP840216.RAedaHJnrCNJ8i0-ShmBy8VorcrXRiLgwcf8t4lTLP9Fs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP840216.RAedaHJnrCNJ8i0-ShmBy8VorcrXRiLgwcf8t4lTLP9Fs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP840216.RAedaHJnrCNJ8i0-ShmBy8VorcrXRiLgwcf8t4lTLP9Fs130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP840216.RAedaHJnrCNJ8i0-ShmBy8VorcrXRiLgwcf8t4lTLP9Fs130_provenance.