Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1031274.RA0vgczkoDloP_N0zCiFlqbPufrMJFbM0hHQh9Ym1iduk130_assertion> ?p ?o ?g. }
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- NP1031274.RA0vgczkoDloP_N0zCiFlqbPufrMJFbM0hHQh9Ym1iduk130_assertion type Assertion NP1031274.RA0vgczkoDloP_N0zCiFlqbPufrMJFbM0hHQh9Ym1iduk130_head.
- NP1031274.RA0vgczkoDloP_N0zCiFlqbPufrMJFbM0hHQh9Ym1iduk130_assertion description "[Mutations in the PFN1 gene are not a common cause in patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration in France.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1031274.RA0vgczkoDloP_N0zCiFlqbPufrMJFbM0hHQh9Ym1iduk130_provenance.
- NP1031274.RA0vgczkoDloP_N0zCiFlqbPufrMJFbM0hHQh9Ym1iduk130_assertion evidence source_evidence_literature NP1031274.RA0vgczkoDloP_N0zCiFlqbPufrMJFbM0hHQh9Ym1iduk130_provenance.
- NP1031274.RA0vgczkoDloP_N0zCiFlqbPufrMJFbM0hHQh9Ym1iduk130_assertion SIO_000772 23182804 NP1031274.RA0vgczkoDloP_N0zCiFlqbPufrMJFbM0hHQh9Ym1iduk130_provenance.
- NP1031274.RA0vgczkoDloP_N0zCiFlqbPufrMJFbM0hHQh9Ym1iduk130_assertion wasDerivedFrom befree-2016 NP1031274.RA0vgczkoDloP_N0zCiFlqbPufrMJFbM0hHQh9Ym1iduk130_provenance.
- NP1031274.RA0vgczkoDloP_N0zCiFlqbPufrMJFbM0hHQh9Ym1iduk130_assertion wasGeneratedBy ECO_0000203 NP1031274.RA0vgczkoDloP_N0zCiFlqbPufrMJFbM0hHQh9Ym1iduk130_provenance.