Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_provenance.
- NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_assertion description "[Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_provenance.
- NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_assertion evidence source_evidence_curated NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_provenance.
- NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_assertion SIO_000772 23768516 NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_provenance.
- NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_assertion wasDerivedFrom uniprot-20150221 NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_provenance.
- NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_assertion wasGeneratedBy ECO_0000218 NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_provenance.