Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP430733.RAVxtqNKJamLU18VJAmNXJ-WwSixGxNgfpJ4Q3XRsvO4s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP430733.RAVxtqNKJamLU18VJAmNXJ-WwSixGxNgfpJ4Q3XRsvO4s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP430733.RAVxtqNKJamLU18VJAmNXJ-WwSixGxNgfpJ4Q3XRsvO4s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP430733.RAVxtqNKJamLU18VJAmNXJ-WwSixGxNgfpJ4Q3XRsvO4s130_provenance.
- NP430733.RAVxtqNKJamLU18VJAmNXJ-WwSixGxNgfpJ4Q3XRsvO4s130_assertion description "[The method was developed on single blood leukocytes, obtained from healthy controls and an adult SMA type III patient with a known homozygous deletion of SMN1 exon 7 and 8.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430733.RAVxtqNKJamLU18VJAmNXJ-WwSixGxNgfpJ4Q3XRsvO4s130_provenance.
- NP430733.RAVxtqNKJamLU18VJAmNXJ-WwSixGxNgfpJ4Q3XRsvO4s130_assertion evidence source_evidence_literature NP430733.RAVxtqNKJamLU18VJAmNXJ-WwSixGxNgfpJ4Q3XRsvO4s130_provenance.
- NP430733.RAVxtqNKJamLU18VJAmNXJ-WwSixGxNgfpJ4Q3XRsvO4s130_assertion SIO_000772 14764971 NP430733.RAVxtqNKJamLU18VJAmNXJ-WwSixGxNgfpJ4Q3XRsvO4s130_provenance.
- NP430733.RAVxtqNKJamLU18VJAmNXJ-WwSixGxNgfpJ4Q3XRsvO4s130_assertion wasDerivedFrom befree-2016 NP430733.RAVxtqNKJamLU18VJAmNXJ-WwSixGxNgfpJ4Q3XRsvO4s130_provenance.
- NP430733.RAVxtqNKJamLU18VJAmNXJ-WwSixGxNgfpJ4Q3XRsvO4s130_assertion wasGeneratedBy ECO_0000203 NP430733.RAVxtqNKJamLU18VJAmNXJ-WwSixGxNgfpJ4Q3XRsvO4s130_provenance.
- befree-2016 importedOn "2016-02-19" NP430733.RAVxtqNKJamLU18VJAmNXJ-WwSixGxNgfpJ4Q3XRsvO4s130_provenance.