Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP9443.RAdgX95nv4eSqAg4SfrMZApejDVHLwH3YTvCLMVV2WImM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP9443.RAdgX95nv4eSqAg4SfrMZApejDVHLwH3YTvCLMVV2WImM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP9443.RAdgX95nv4eSqAg4SfrMZApejDVHLwH3YTvCLMVV2WImM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP9443.RAdgX95nv4eSqAg4SfrMZApejDVHLwH3YTvCLMVV2WImM130_provenance.
- NP9443.RAdgX95nv4eSqAg4SfrMZApejDVHLwH3YTvCLMVV2WImM130_assertion description "[Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9443.RAdgX95nv4eSqAg4SfrMZApejDVHLwH3YTvCLMVV2WImM130_provenance.
- NP9443.RAdgX95nv4eSqAg4SfrMZApejDVHLwH3YTvCLMVV2WImM130_assertion evidence source_evidence_curated NP9443.RAdgX95nv4eSqAg4SfrMZApejDVHLwH3YTvCLMVV2WImM130_provenance.
- NP9443.RAdgX95nv4eSqAg4SfrMZApejDVHLwH3YTvCLMVV2WImM130_assertion SIO_000772 9233560 NP9443.RAdgX95nv4eSqAg4SfrMZApejDVHLwH3YTvCLMVV2WImM130_provenance.
- NP9443.RAdgX95nv4eSqAg4SfrMZApejDVHLwH3YTvCLMVV2WImM130_assertion wasDerivedFrom uniprot-2016 NP9443.RAdgX95nv4eSqAg4SfrMZApejDVHLwH3YTvCLMVV2WImM130_provenance.
- NP9443.RAdgX95nv4eSqAg4SfrMZApejDVHLwH3YTvCLMVV2WImM130_assertion wasGeneratedBy ECO_0000218 NP9443.RAdgX95nv4eSqAg4SfrMZApejDVHLwH3YTvCLMVV2WImM130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP9443.RAdgX95nv4eSqAg4SfrMZApejDVHLwH3YTvCLMVV2WImM130_provenance.