Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP697799.RAHDJOtXC_akKdPkvBGfTliHWZ9Qq02FC4MCRPfOPesIA130_assertion> ?p ?o ?g. }
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- NP697799.RAHDJOtXC_akKdPkvBGfTliHWZ9Qq02FC4MCRPfOPesIA130_assertion type Assertion NP697799.RAHDJOtXC_akKdPkvBGfTliHWZ9Qq02FC4MCRPfOPesIA130_head.
- NP697799.RAHDJOtXC_akKdPkvBGfTliHWZ9Qq02FC4MCRPfOPesIA130_assertion description "[A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697799.RAHDJOtXC_akKdPkvBGfTliHWZ9Qq02FC4MCRPfOPesIA130_provenance.
- NP697799.RAHDJOtXC_akKdPkvBGfTliHWZ9Qq02FC4MCRPfOPesIA130_assertion evidence source_evidence_literature NP697799.RAHDJOtXC_akKdPkvBGfTliHWZ9Qq02FC4MCRPfOPesIA130_provenance.
- NP697799.RAHDJOtXC_akKdPkvBGfTliHWZ9Qq02FC4MCRPfOPesIA130_assertion SIO_000772 20593214 NP697799.RAHDJOtXC_akKdPkvBGfTliHWZ9Qq02FC4MCRPfOPesIA130_provenance.
- NP697799.RAHDJOtXC_akKdPkvBGfTliHWZ9Qq02FC4MCRPfOPesIA130_assertion wasDerivedFrom befree-20140225 NP697799.RAHDJOtXC_akKdPkvBGfTliHWZ9Qq02FC4MCRPfOPesIA130_provenance.
- NP697799.RAHDJOtXC_akKdPkvBGfTliHWZ9Qq02FC4MCRPfOPesIA130_assertion wasGeneratedBy ECO_0000203 NP697799.RAHDJOtXC_akKdPkvBGfTliHWZ9Qq02FC4MCRPfOPesIA130_provenance.