Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_assertion type Assertion NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_head.
- 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.