Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP571031.RAcOWI1tpKoSsXUzpikU0m8KaIzwtUt632XRzHKv3_CYA130_assertion> ?p ?o ?g. }
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- NP571031.RAcOWI1tpKoSsXUzpikU0m8KaIzwtUt632XRzHKv3_CYA130_assertion type Assertion NP571031.RAcOWI1tpKoSsXUzpikU0m8KaIzwtUt632XRzHKv3_CYA130_head.
- NP571031.RAcOWI1tpKoSsXUzpikU0m8KaIzwtUt632XRzHKv3_CYA130_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." NP571031.RAcOWI1tpKoSsXUzpikU0m8KaIzwtUt632XRzHKv3_CYA130_provenance.
- NP571031.RAcOWI1tpKoSsXUzpikU0m8KaIzwtUt632XRzHKv3_CYA130_assertion evidence source_evidence_literature NP571031.RAcOWI1tpKoSsXUzpikU0m8KaIzwtUt632XRzHKv3_CYA130_provenance.
- NP571031.RAcOWI1tpKoSsXUzpikU0m8KaIzwtUt632XRzHKv3_CYA130_assertion SIO_000772 20377183 NP571031.RAcOWI1tpKoSsXUzpikU0m8KaIzwtUt632XRzHKv3_CYA130_provenance.
- NP571031.RAcOWI1tpKoSsXUzpikU0m8KaIzwtUt632XRzHKv3_CYA130_assertion wasDerivedFrom befree-20150227 NP571031.RAcOWI1tpKoSsXUzpikU0m8KaIzwtUt632XRzHKv3_CYA130_provenance.
- NP571031.RAcOWI1tpKoSsXUzpikU0m8KaIzwtUt632XRzHKv3_CYA130_assertion wasGeneratedBy ECO_0000203 NP571031.RAcOWI1tpKoSsXUzpikU0m8KaIzwtUt632XRzHKv3_CYA130_provenance.