Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP8215.RAuZo_ssLhif_50lkwAajp4ISSOtkBql2D1FyNR6X8GYQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP8215.RAuZo_ssLhif_50lkwAajp4ISSOtkBql2D1FyNR6X8GYQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8215.RAuZo_ssLhif_50lkwAajp4ISSOtkBql2D1FyNR6X8GYQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8215.RAuZo_ssLhif_50lkwAajp4ISSOtkBql2D1FyNR6X8GYQ130_provenance.
- NP8215.RAuZo_ssLhif_50lkwAajp4ISSOtkBql2D1FyNR6X8GYQ130_assertion description "[Identification of a point mutation resulting in a heat-labile adenosine deaminase (ADA) in two unrelated children with partial ADA deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8215.RAuZo_ssLhif_50lkwAajp4ISSOtkBql2D1FyNR6X8GYQ130_provenance.
- NP8215.RAuZo_ssLhif_50lkwAajp4ISSOtkBql2D1FyNR6X8GYQ130_assertion evidence source_evidence_curated NP8215.RAuZo_ssLhif_50lkwAajp4ISSOtkBql2D1FyNR6X8GYQ130_provenance.
- NP8215.RAuZo_ssLhif_50lkwAajp4ISSOtkBql2D1FyNR6X8GYQ130_assertion SIO_000772 2783588 NP8215.RAuZo_ssLhif_50lkwAajp4ISSOtkBql2D1FyNR6X8GYQ130_provenance.
- NP8215.RAuZo_ssLhif_50lkwAajp4ISSOtkBql2D1FyNR6X8GYQ130_assertion wasDerivedFrom uniprot-2016 NP8215.RAuZo_ssLhif_50lkwAajp4ISSOtkBql2D1FyNR6X8GYQ130_provenance.
- NP8215.RAuZo_ssLhif_50lkwAajp4ISSOtkBql2D1FyNR6X8GYQ130_assertion wasGeneratedBy ECO_0000218 NP8215.RAuZo_ssLhif_50lkwAajp4ISSOtkBql2D1FyNR6X8GYQ130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP8215.RAuZo_ssLhif_50lkwAajp4ISSOtkBql2D1FyNR6X8GYQ130_provenance.