Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP175594.RAkb65DiBd_lHbel-G_oJna--5kS0zSjhvSAdGQoMd9Js130_assertion> ?p ?o ?g. }
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- NP175594.RAkb65DiBd_lHbel-G_oJna--5kS0zSjhvSAdGQoMd9Js130_assertion type Assertion NP175594.RAkb65DiBd_lHbel-G_oJna--5kS0zSjhvSAdGQoMd9Js130_head.
- NP175594.RAkb65DiBd_lHbel-G_oJna--5kS0zSjhvSAdGQoMd9Js130_assertion description "[The classical form of severe spinal muscular atrophy (SMA type 1; Werdnig-Hoffmann disease) has a very consistent clinical phenotype that is well recognized by paediatricians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP175594.RAkb65DiBd_lHbel-G_oJna--5kS0zSjhvSAdGQoMd9Js130_provenance.
- NP175594.RAkb65DiBd_lHbel-G_oJna--5kS0zSjhvSAdGQoMd9Js130_assertion evidence source_evidence_literature NP175594.RAkb65DiBd_lHbel-G_oJna--5kS0zSjhvSAdGQoMd9Js130_provenance.
- NP175594.RAkb65DiBd_lHbel-G_oJna--5kS0zSjhvSAdGQoMd9Js130_assertion SIO_000772 10700538 NP175594.RAkb65DiBd_lHbel-G_oJna--5kS0zSjhvSAdGQoMd9Js130_provenance.
- NP175594.RAkb65DiBd_lHbel-G_oJna--5kS0zSjhvSAdGQoMd9Js130_assertion wasDerivedFrom befree-20140225 NP175594.RAkb65DiBd_lHbel-G_oJna--5kS0zSjhvSAdGQoMd9Js130_provenance.
- NP175594.RAkb65DiBd_lHbel-G_oJna--5kS0zSjhvSAdGQoMd9Js130_assertion wasGeneratedBy ECO_0000203 NP175594.RAkb65DiBd_lHbel-G_oJna--5kS0zSjhvSAdGQoMd9Js130_provenance.