Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1111436.RAAVJen9J0gz0esoPXWweyXY4ztGK4yOqxGMtKnlkHrn8130_assertion> ?p ?o ?g. }
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- NP1111436.RAAVJen9J0gz0esoPXWweyXY4ztGK4yOqxGMtKnlkHrn8130_assertion type Assertion NP1111436.RAAVJen9J0gz0esoPXWweyXY4ztGK4yOqxGMtKnlkHrn8130_head.
- NP1111436.RAAVJen9J0gz0esoPXWweyXY4ztGK4yOqxGMtKnlkHrn8130_assertion description "[To evaluate the frequency of SQSTM1 mutations, we sequenced this gene in a cohort of patients with FTD or FTD-ALS, with no mutations in known FTD and ALS genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1111436.RAAVJen9J0gz0esoPXWweyXY4ztGK4yOqxGMtKnlkHrn8130_provenance.
- NP1111436.RAAVJen9J0gz0esoPXWweyXY4ztGK4yOqxGMtKnlkHrn8130_assertion evidence source_evidence_literature NP1111436.RAAVJen9J0gz0esoPXWweyXY4ztGK4yOqxGMtKnlkHrn8130_provenance.
- NP1111436.RAAVJen9J0gz0esoPXWweyXY4ztGK4yOqxGMtKnlkHrn8130_assertion SIO_000772 24042580 NP1111436.RAAVJen9J0gz0esoPXWweyXY4ztGK4yOqxGMtKnlkHrn8130_provenance.
- NP1111436.RAAVJen9J0gz0esoPXWweyXY4ztGK4yOqxGMtKnlkHrn8130_assertion wasDerivedFrom befree-2016 NP1111436.RAAVJen9J0gz0esoPXWweyXY4ztGK4yOqxGMtKnlkHrn8130_provenance.
- NP1111436.RAAVJen9J0gz0esoPXWweyXY4ztGK4yOqxGMtKnlkHrn8130_assertion wasGeneratedBy ECO_0000203 NP1111436.RAAVJen9J0gz0esoPXWweyXY4ztGK4yOqxGMtKnlkHrn8130_provenance.