Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP872928.RASHmyrxwhUi179ziiIIRZzE_3LSxmzNO2Y5G377YDLbU130_assertion> ?p ?o ?g. }
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- NP872928.RASHmyrxwhUi179ziiIIRZzE_3LSxmzNO2Y5G377YDLbU130_assertion type Assertion NP872928.RASHmyrxwhUi179ziiIIRZzE_3LSxmzNO2Y5G377YDLbU130_head.
- NP872928.RASHmyrxwhUi179ziiIIRZzE_3LSxmzNO2Y5G377YDLbU130_assertion wasGeneratedBy ECO_0000203 NP872928.RASHmyrxwhUi179ziiIIRZzE_3LSxmzNO2Y5G377YDLbU130_provenance.
- NP872928.RASHmyrxwhUi179ziiIIRZzE_3LSxmzNO2Y5G377YDLbU130_assertion wasDerivedFrom befree-20150227 NP872928.RASHmyrxwhUi179ziiIIRZzE_3LSxmzNO2Y5G377YDLbU130_provenance.
- NP872928.RASHmyrxwhUi179ziiIIRZzE_3LSxmzNO2Y5G377YDLbU130_assertion SIO_000772 24439481 NP872928.RASHmyrxwhUi179ziiIIRZzE_3LSxmzNO2Y5G377YDLbU130_provenance.
- NP872928.RASHmyrxwhUi179ziiIIRZzE_3LSxmzNO2Y5G377YDLbU130_assertion evidence source_evidence_literature NP872928.RASHmyrxwhUi179ziiIIRZzE_3LSxmzNO2Y5G377YDLbU130_provenance.
- NP872928.RASHmyrxwhUi179ziiIIRZzE_3LSxmzNO2Y5G377YDLbU130_assertion description "[Mutations in C9ORF72, SOD1, TARDBP, and FUS genes account for approximately two-third of familial cases and 5% of sporadic amyotrophic lateral sclerosis (ALS) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872928.RASHmyrxwhUi179ziiIIRZzE_3LSxmzNO2Y5G377YDLbU130_provenance.