Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP282645.RAKa4c5AH5Ev7FE4TVbRnAa8NFSR3wxsz9dFJ1hsYVdqg130_assertion> ?p ?o ?g. }
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- NP282645.RAKa4c5AH5Ev7FE4TVbRnAa8NFSR3wxsz9dFJ1hsYVdqg130_assertion type Assertion NP282645.RAKa4c5AH5Ev7FE4TVbRnAa8NFSR3wxsz9dFJ1hsYVdqg130_head.
- NP282645.RAKa4c5AH5Ev7FE4TVbRnAa8NFSR3wxsz9dFJ1hsYVdqg130_assertion description "[Hereditary spastic paraparesis (HPS) linked to mutations in the spastin gene (SPG4) is considered to be a pure form of spastic hereditary paraparesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP282645.RAKa4c5AH5Ev7FE4TVbRnAa8NFSR3wxsz9dFJ1hsYVdqg130_provenance.
- NP282645.RAKa4c5AH5Ev7FE4TVbRnAa8NFSR3wxsz9dFJ1hsYVdqg130_assertion evidence source_evidence_literature NP282645.RAKa4c5AH5Ev7FE4TVbRnAa8NFSR3wxsz9dFJ1hsYVdqg130_provenance.
- NP282645.RAKa4c5AH5Ev7FE4TVbRnAa8NFSR3wxsz9dFJ1hsYVdqg130_assertion SIO_000772 19289482 NP282645.RAKa4c5AH5Ev7FE4TVbRnAa8NFSR3wxsz9dFJ1hsYVdqg130_provenance.
- NP282645.RAKa4c5AH5Ev7FE4TVbRnAa8NFSR3wxsz9dFJ1hsYVdqg130_assertion wasDerivedFrom befree-20140225 NP282645.RAKa4c5AH5Ev7FE4TVbRnAa8NFSR3wxsz9dFJ1hsYVdqg130_provenance.
- NP282645.RAKa4c5AH5Ev7FE4TVbRnAa8NFSR3wxsz9dFJ1hsYVdqg130_assertion wasGeneratedBy ECO_0000203 NP282645.RAKa4c5AH5Ev7FE4TVbRnAa8NFSR3wxsz9dFJ1hsYVdqg130_provenance.