Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_assertion> ?p ?o ?g. }
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- NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_assertion type Assertion NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_head.
- NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_assertion description "[The Pro56Ser mutation in the human VAPB MSP domain causes a familial amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_provenance.
- NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_assertion evidence source_evidence_literature NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_provenance.
- NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_assertion SIO_000772 20377183 NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_provenance.
- NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_assertion wasDerivedFrom befree-20150227 NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_provenance.
- NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_assertion wasGeneratedBy ECO_0000203 NP959834.RAr5qHCa0gHjtX_jlAKBJKlH4TtKNpjwoN-XRitTY4YXc130_provenance.