Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP697799.RAHDJOtXC_akKdPkvBGfTliHWZ9Qq02FC4MCRPfOPesIA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP697799.RAHDJOtXC_akKdPkvBGfTliHWZ9Qq02FC4MCRPfOPesIA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697799.RAHDJOtXC_akKdPkvBGfTliHWZ9Qq02FC4MCRPfOPesIA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697799.RAHDJOtXC_akKdPkvBGfTliHWZ9Qq02FC4MCRPfOPesIA130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP697799.RAHDJOtXC_akKdPkvBGfTliHWZ9Qq02FC4MCRPfOPesIA130_provenance.