Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_assertion> ?p ?o ?g. }
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- NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_assertion type Assertion NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_head.
- NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_assertion wasGeneratedBy ECO_0000218 NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_provenance.
- NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_assertion wasDerivedFrom ctd_human-2016 NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_provenance.
- NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_assertion SIO_000772 11951178 NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_provenance.
- NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_assertion evidence source_evidence_curated NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_provenance.
- NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_assertion description "[Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP11922.RAu06b79HrQFTTeRQqxDOY_lpy6OhM5dbO2_JrbmNEDUA130_provenance.