Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP10918.RA7gKdKQjMcg_JSgwv-sieF6-b8YExlH6rL3_891wVDZE130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP10918.RA7gKdKQjMcg_JSgwv-sieF6-b8YExlH6rL3_891wVDZE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP10918.RA7gKdKQjMcg_JSgwv-sieF6-b8YExlH6rL3_891wVDZE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP10918.RA7gKdKQjMcg_JSgwv-sieF6-b8YExlH6rL3_891wVDZE130_provenance.
- NP10918.RA7gKdKQjMcg_JSgwv-sieF6-b8YExlH6rL3_891wVDZE130_assertion description "[Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP10918.RA7gKdKQjMcg_JSgwv-sieF6-b8YExlH6rL3_891wVDZE130_provenance.
- NP10918.RA7gKdKQjMcg_JSgwv-sieF6-b8YExlH6rL3_891wVDZE130_assertion evidence source_evidence_curated NP10918.RA7gKdKQjMcg_JSgwv-sieF6-b8YExlH6rL3_891wVDZE130_provenance.
- NP10918.RA7gKdKQjMcg_JSgwv-sieF6-b8YExlH6rL3_891wVDZE130_assertion SIO_000772 10973259 NP10918.RA7gKdKQjMcg_JSgwv-sieF6-b8YExlH6rL3_891wVDZE130_provenance.
- NP10918.RA7gKdKQjMcg_JSgwv-sieF6-b8YExlH6rL3_891wVDZE130_assertion wasDerivedFrom ctd_human-2016 NP10918.RA7gKdKQjMcg_JSgwv-sieF6-b8YExlH6rL3_891wVDZE130_provenance.
- NP10918.RA7gKdKQjMcg_JSgwv-sieF6-b8YExlH6rL3_891wVDZE130_assertion wasGeneratedBy ECO_0000218 NP10918.RA7gKdKQjMcg_JSgwv-sieF6-b8YExlH6rL3_891wVDZE130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP10918.RA7gKdKQjMcg_JSgwv-sieF6-b8YExlH6rL3_891wVDZE130_provenance.