Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_provenance.
- NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_assertion description "[Partial SPAST deletions represent an underestimated cause of autosomal dominant hereditary spastic paraplegia/SPAST deletions are likely to act via haploinsufficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_provenance.
- NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_assertion evidence source_evidence_literature NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_provenance.
- NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_assertion SIO_000772 17035675 NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_provenance.
- NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_assertion wasDerivedFrom lhgdn-20090331 NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_provenance.
- NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_assertion wasGeneratedBy ECO_0000203 NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP220226.RACRB6YCHeFzvJV0o1fZtMXNNtvgbfdu8KabI6uhiQT4E130_provenance.