Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_provenance.
- NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_assertion wasGeneratedBy ECO_0000203 NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_provenance.
- NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_assertion wasDerivedFrom befree-20150227 NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_provenance.
- NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_assertion SIO_000772 18853458 NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_provenance.
- NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_assertion evidence source_evidence_literature NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_provenance.
- NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_assertion description "[Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_provenance.