Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP710139.RAbp7Vr2qDQ0aDrWcAtO3686ykLeA1G2aNPLp5xqEDHUY130_assertion> ?p ?o ?g. }
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- NP710139.RAbp7Vr2qDQ0aDrWcAtO3686ykLeA1G2aNPLp5xqEDHUY130_assertion type Assertion NP710139.RAbp7Vr2qDQ0aDrWcAtO3686ykLeA1G2aNPLp5xqEDHUY130_head.
- NP710139.RAbp7Vr2qDQ0aDrWcAtO3686ykLeA1G2aNPLp5xqEDHUY130_assertion description "[Mutations in the SPG7 gene encoding a mitochondrial protein termed paraplegin, are responsible for a recessive form of hereditary spastic paraparesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710139.RAbp7Vr2qDQ0aDrWcAtO3686ykLeA1G2aNPLp5xqEDHUY130_provenance.
- NP710139.RAbp7Vr2qDQ0aDrWcAtO3686ykLeA1G2aNPLp5xqEDHUY130_assertion evidence source_evidence_literature NP710139.RAbp7Vr2qDQ0aDrWcAtO3686ykLeA1G2aNPLp5xqEDHUY130_provenance.
- NP710139.RAbp7Vr2qDQ0aDrWcAtO3686ykLeA1G2aNPLp5xqEDHUY130_assertion SIO_000772 18200586 NP710139.RAbp7Vr2qDQ0aDrWcAtO3686ykLeA1G2aNPLp5xqEDHUY130_provenance.
- NP710139.RAbp7Vr2qDQ0aDrWcAtO3686ykLeA1G2aNPLp5xqEDHUY130_assertion wasDerivedFrom befree-20150227 NP710139.RAbp7Vr2qDQ0aDrWcAtO3686ykLeA1G2aNPLp5xqEDHUY130_provenance.
- NP710139.RAbp7Vr2qDQ0aDrWcAtO3686ykLeA1G2aNPLp5xqEDHUY130_assertion wasGeneratedBy ECO_0000203 NP710139.RAbp7Vr2qDQ0aDrWcAtO3686ykLeA1G2aNPLp5xqEDHUY130_provenance.