Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP932860.RAbsCHeoHTu151fx5LkwYPk7JlLjM0EttVeTHKWzCUMV4130_assertion> ?p ?o ?g. }
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- NP932860.RAbsCHeoHTu151fx5LkwYPk7JlLjM0EttVeTHKWzCUMV4130_assertion type Assertion NP932860.RAbsCHeoHTu151fx5LkwYPk7JlLjM0EttVeTHKWzCUMV4130_head.
- NP932860.RAbsCHeoHTu151fx5LkwYPk7JlLjM0EttVeTHKWzCUMV4130_assertion wasGeneratedBy ECO_0000203 NP932860.RAbsCHeoHTu151fx5LkwYPk7JlLjM0EttVeTHKWzCUMV4130_provenance.
- NP932860.RAbsCHeoHTu151fx5LkwYPk7JlLjM0EttVeTHKWzCUMV4130_assertion wasDerivedFrom befree-20150227 NP932860.RAbsCHeoHTu151fx5LkwYPk7JlLjM0EttVeTHKWzCUMV4130_provenance.
- NP932860.RAbsCHeoHTu151fx5LkwYPk7JlLjM0EttVeTHKWzCUMV4130_assertion SIO_000772 17855450 NP932860.RAbsCHeoHTu151fx5LkwYPk7JlLjM0EttVeTHKWzCUMV4130_provenance.
- NP932860.RAbsCHeoHTu151fx5LkwYPk7JlLjM0EttVeTHKWzCUMV4130_assertion evidence source_evidence_literature NP932860.RAbsCHeoHTu151fx5LkwYPk7JlLjM0EttVeTHKWzCUMV4130_provenance.
- NP932860.RAbsCHeoHTu151fx5LkwYPk7JlLjM0EttVeTHKWzCUMV4130_assertion description "[Mutations in Alsin are associated with chronic juvenile amyotrophic lateral sclerosis (ALS2), juvenile primary lateral sclerosis and infantile-onset ascending spastic paralysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932860.RAbsCHeoHTu151fx5LkwYPk7JlLjM0EttVeTHKWzCUMV4130_provenance.