Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_assertion> ?p ?o ?g. }
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- NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_assertion type Assertion NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_head.
- NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_assertion description "[Mutations in the SPG7 gene, which encodes paraplegin, are responsible for an autosomal recessive hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_provenance.
- NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_assertion evidence source_evidence_literature NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_provenance.
- NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_assertion SIO_000772 16534102 NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_provenance.
- NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_assertion wasDerivedFrom befree-2016 NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_provenance.
- NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_assertion wasGeneratedBy ECO_0000203 NP539955.RAXMqFiWgYnNJRIPn4cC7kZwUsqeoVhsraPdIfFvuJPmI130_provenance.