Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP9972.RAQDsJ7mpEYTgOGkY0H_gFX_c64W-PraMqdl_BNLkTCss130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP9972.RAQDsJ7mpEYTgOGkY0H_gFX_c64W-PraMqdl_BNLkTCss130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP9972.RAQDsJ7mpEYTgOGkY0H_gFX_c64W-PraMqdl_BNLkTCss130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP9972.RAQDsJ7mpEYTgOGkY0H_gFX_c64W-PraMqdl_BNLkTCss130_provenance.
- NP9972.RAQDsJ7mpEYTgOGkY0H_gFX_c64W-PraMqdl_BNLkTCss130_assertion description "[No obvious correlation was observed between the position or type of the RSK2 mutations and the severity or particular clinical features of CLS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9972.RAQDsJ7mpEYTgOGkY0H_gFX_c64W-PraMqdl_BNLkTCss130_provenance.
- NP9972.RAQDsJ7mpEYTgOGkY0H_gFX_c64W-PraMqdl_BNLkTCss130_assertion evidence source_evidence_curated NP9972.RAQDsJ7mpEYTgOGkY0H_gFX_c64W-PraMqdl_BNLkTCss130_provenance.
- NP9972.RAQDsJ7mpEYTgOGkY0H_gFX_c64W-PraMqdl_BNLkTCss130_assertion SIO_000772 9837815 NP9972.RAQDsJ7mpEYTgOGkY0H_gFX_c64W-PraMqdl_BNLkTCss130_provenance.
- NP9972.RAQDsJ7mpEYTgOGkY0H_gFX_c64W-PraMqdl_BNLkTCss130_assertion wasDerivedFrom uniprot-2016 NP9972.RAQDsJ7mpEYTgOGkY0H_gFX_c64W-PraMqdl_BNLkTCss130_provenance.
- NP9972.RAQDsJ7mpEYTgOGkY0H_gFX_c64W-PraMqdl_BNLkTCss130_assertion wasGeneratedBy ECO_0000218 NP9972.RAQDsJ7mpEYTgOGkY0H_gFX_c64W-PraMqdl_BNLkTCss130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP9972.RAQDsJ7mpEYTgOGkY0H_gFX_c64W-PraMqdl_BNLkTCss130_provenance.