Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_provenance.
- befree-2016 importedOn "2016-02-19" NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_provenance.
- NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_assertion wasGeneratedBy ECO_0000203 NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_provenance.
- NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_assertion wasDerivedFrom befree-2016 NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_provenance.
- NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_assertion SIO_000772 18853458 NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_provenance.
- NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_assertion evidence source_evidence_literature NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_provenance.
- NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_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." NP697782.RANM4FSzBG5TV1LK42RUWDPA0XntRA2iyssmNOhhe9jIg130_provenance.