Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP710147.RAmJPQF7AXNBcF9uGy_TCXGUpQw_SEdHTgeX9aqfJkPJw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP710147.RAmJPQF7AXNBcF9uGy_TCXGUpQw_SEdHTgeX9aqfJkPJw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710147.RAmJPQF7AXNBcF9uGy_TCXGUpQw_SEdHTgeX9aqfJkPJw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710147.RAmJPQF7AXNBcF9uGy_TCXGUpQw_SEdHTgeX9aqfJkPJw130_provenance.
- NP710147.RAmJPQF7AXNBcF9uGy_TCXGUpQw_SEdHTgeX9aqfJkPJw130_assertion description "[Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710147.RAmJPQF7AXNBcF9uGy_TCXGUpQw_SEdHTgeX9aqfJkPJw130_provenance.
- NP710147.RAmJPQF7AXNBcF9uGy_TCXGUpQw_SEdHTgeX9aqfJkPJw130_assertion evidence source_evidence_literature NP710147.RAmJPQF7AXNBcF9uGy_TCXGUpQw_SEdHTgeX9aqfJkPJw130_provenance.
- NP710147.RAmJPQF7AXNBcF9uGy_TCXGUpQw_SEdHTgeX9aqfJkPJw130_assertion SIO_000772 16534102 NP710147.RAmJPQF7AXNBcF9uGy_TCXGUpQw_SEdHTgeX9aqfJkPJw130_provenance.
- NP710147.RAmJPQF7AXNBcF9uGy_TCXGUpQw_SEdHTgeX9aqfJkPJw130_assertion wasDerivedFrom befree-20150227 NP710147.RAmJPQF7AXNBcF9uGy_TCXGUpQw_SEdHTgeX9aqfJkPJw130_provenance.
- NP710147.RAmJPQF7AXNBcF9uGy_TCXGUpQw_SEdHTgeX9aqfJkPJw130_assertion wasGeneratedBy ECO_0000203 NP710147.RAmJPQF7AXNBcF9uGy_TCXGUpQw_SEdHTgeX9aqfJkPJw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP710147.RAmJPQF7AXNBcF9uGy_TCXGUpQw_SEdHTgeX9aqfJkPJw130_provenance.