Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP19918.RAWmZsuiAlteMy0YDXvm8Ouwpy3EVRNYGXTfWMcSlEpxo130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP19918.RAWmZsuiAlteMy0YDXvm8Ouwpy3EVRNYGXTfWMcSlEpxo130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP19918.RAWmZsuiAlteMy0YDXvm8Ouwpy3EVRNYGXTfWMcSlEpxo130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP19918.RAWmZsuiAlteMy0YDXvm8Ouwpy3EVRNYGXTfWMcSlEpxo130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP19918.RAWmZsuiAlteMy0YDXvm8Ouwpy3EVRNYGXTfWMcSlEpxo130_provenance.
- NP19918.RAWmZsuiAlteMy0YDXvm8Ouwpy3EVRNYGXTfWMcSlEpxo130_assertion wasGeneratedBy ECO_0000218 NP19918.RAWmZsuiAlteMy0YDXvm8Ouwpy3EVRNYGXTfWMcSlEpxo130_provenance.
- NP19918.RAWmZsuiAlteMy0YDXvm8Ouwpy3EVRNYGXTfWMcSlEpxo130_assertion wasDerivedFrom ctd_human-20150221 NP19918.RAWmZsuiAlteMy0YDXvm8Ouwpy3EVRNYGXTfWMcSlEpxo130_provenance.
- NP19918.RAWmZsuiAlteMy0YDXvm8Ouwpy3EVRNYGXTfWMcSlEpxo130_assertion SIO_000772 12022040 NP19918.RAWmZsuiAlteMy0YDXvm8Ouwpy3EVRNYGXTfWMcSlEpxo130_provenance.
- NP19918.RAWmZsuiAlteMy0YDXvm8Ouwpy3EVRNYGXTfWMcSlEpxo130_assertion evidence source_evidence_curated NP19918.RAWmZsuiAlteMy0YDXvm8Ouwpy3EVRNYGXTfWMcSlEpxo130_provenance.
- NP19918.RAWmZsuiAlteMy0YDXvm8Ouwpy3EVRNYGXTfWMcSlEpxo130_assertion description "[Familial deafness, congenital heart defects, and posterior embryotoxon caused by cysteine substitution in the first epidermal-growth-factor-like domain of jagged 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP19918.RAWmZsuiAlteMy0YDXvm8Ouwpy3EVRNYGXTfWMcSlEpxo130_provenance.