Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP668557.RAOPGH5gfBLAOi09dTjLUErAyFmTl8VqHs4cxhuCVSLEc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP668557.RAOPGH5gfBLAOi09dTjLUErAyFmTl8VqHs4cxhuCVSLEc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668557.RAOPGH5gfBLAOi09dTjLUErAyFmTl8VqHs4cxhuCVSLEc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668557.RAOPGH5gfBLAOi09dTjLUErAyFmTl8VqHs4cxhuCVSLEc130_provenance.
- NP668557.RAOPGH5gfBLAOi09dTjLUErAyFmTl8VqHs4cxhuCVSLEc130_assertion description "[HSP is a genetically diverse group of disorders characterized by insidiously progressive spastic weakness in the legs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668557.RAOPGH5gfBLAOi09dTjLUErAyFmTl8VqHs4cxhuCVSLEc130_provenance.
- NP668557.RAOPGH5gfBLAOi09dTjLUErAyFmTl8VqHs4cxhuCVSLEc130_assertion evidence source_evidence_literature NP668557.RAOPGH5gfBLAOi09dTjLUErAyFmTl8VqHs4cxhuCVSLEc130_provenance.
- NP668557.RAOPGH5gfBLAOi09dTjLUErAyFmTl8VqHs4cxhuCVSLEc130_assertion SIO_000772 10408535 NP668557.RAOPGH5gfBLAOi09dTjLUErAyFmTl8VqHs4cxhuCVSLEc130_provenance.
- NP668557.RAOPGH5gfBLAOi09dTjLUErAyFmTl8VqHs4cxhuCVSLEc130_assertion wasDerivedFrom befree-20140225 NP668557.RAOPGH5gfBLAOi09dTjLUErAyFmTl8VqHs4cxhuCVSLEc130_provenance.
- NP668557.RAOPGH5gfBLAOi09dTjLUErAyFmTl8VqHs4cxhuCVSLEc130_assertion wasGeneratedBy ECO_0000203 NP668557.RAOPGH5gfBLAOi09dTjLUErAyFmTl8VqHs4cxhuCVSLEc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP668557.RAOPGH5gfBLAOi09dTjLUErAyFmTl8VqHs4cxhuCVSLEc130_provenance.