Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP233352.RABg-PdRjnJvHSHugZYoMTrI0GaEnONzH5DL7qNpa-1pk130_assertion> ?p ?o ?g. }
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- NP233352.RABg-PdRjnJvHSHugZYoMTrI0GaEnONzH5DL7qNpa-1pk130_assertion type Assertion NP233352.RABg-PdRjnJvHSHugZYoMTrI0GaEnONzH5DL7qNpa-1pk130_head.
- NP233352.RABg-PdRjnJvHSHugZYoMTrI0GaEnONzH5DL7qNpa-1pk130_assertion description "[identification of six novel point mutations and one large intragenic deletion in hereditary spastic paraplegia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP233352.RABg-PdRjnJvHSHugZYoMTrI0GaEnONzH5DL7qNpa-1pk130_provenance.
- NP233352.RABg-PdRjnJvHSHugZYoMTrI0GaEnONzH5DL7qNpa-1pk130_assertion evidence source_evidence_literature NP233352.RABg-PdRjnJvHSHugZYoMTrI0GaEnONzH5DL7qNpa-1pk130_provenance.
- NP233352.RABg-PdRjnJvHSHugZYoMTrI0GaEnONzH5DL7qNpa-1pk130_assertion SIO_000772 18200586 NP233352.RABg-PdRjnJvHSHugZYoMTrI0GaEnONzH5DL7qNpa-1pk130_provenance.
- NP233352.RABg-PdRjnJvHSHugZYoMTrI0GaEnONzH5DL7qNpa-1pk130_assertion wasDerivedFrom lhgdn-20090331 NP233352.RABg-PdRjnJvHSHugZYoMTrI0GaEnONzH5DL7qNpa-1pk130_provenance.
- NP233352.RABg-PdRjnJvHSHugZYoMTrI0GaEnONzH5DL7qNpa-1pk130_assertion wasGeneratedBy ECO_0000203 NP233352.RABg-PdRjnJvHSHugZYoMTrI0GaEnONzH5DL7qNpa-1pk130_provenance.