Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP362131.RAaArYkZvxWNSPq09KIabxx0MbVnPWhkt8AWz1Oyp3j8U130_assertion> ?p ?o ?g. }
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- NP362131.RAaArYkZvxWNSPq09KIabxx0MbVnPWhkt8AWz1Oyp3j8U130_assertion type Assertion NP362131.RAaArYkZvxWNSPq09KIabxx0MbVnPWhkt8AWz1Oyp3j8U130_head.
- NP362131.RAaArYkZvxWNSPq09KIabxx0MbVnPWhkt8AWz1Oyp3j8U130_assertion wasGeneratedBy ECO_0000203 NP362131.RAaArYkZvxWNSPq09KIabxx0MbVnPWhkt8AWz1Oyp3j8U130_provenance.
- NP362131.RAaArYkZvxWNSPq09KIabxx0MbVnPWhkt8AWz1Oyp3j8U130_assertion wasDerivedFrom befree-2016 NP362131.RAaArYkZvxWNSPq09KIabxx0MbVnPWhkt8AWz1Oyp3j8U130_provenance.
- NP362131.RAaArYkZvxWNSPq09KIabxx0MbVnPWhkt8AWz1Oyp3j8U130_assertion SIO_000772 12134148 NP362131.RAaArYkZvxWNSPq09KIabxx0MbVnPWhkt8AWz1Oyp3j8U130_provenance.
- NP362131.RAaArYkZvxWNSPq09KIabxx0MbVnPWhkt8AWz1Oyp3j8U130_assertion evidence source_evidence_literature NP362131.RAaArYkZvxWNSPq09KIabxx0MbVnPWhkt8AWz1Oyp3j8U130_provenance.
- NP362131.RAaArYkZvxWNSPq09KIabxx0MbVnPWhkt8AWz1Oyp3j8U130_assertion description "[SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362131.RAaArYkZvxWNSPq09KIabxx0MbVnPWhkt8AWz1Oyp3j8U130_provenance.