Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_assertion> ?p ?o ?g. }
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- NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_assertion type Assertion NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_head.
- NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_assertion description "[In conclusion, mutation of PRDM16 causes the cardiomyopathy in 1p36 deletion syndrome as well as a proportion of nonsyndromic LVNC and DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_provenance.
- NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_assertion evidence source_evidence_literature NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_provenance.
- NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_assertion SIO_000772 23768516 NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_provenance.
- NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_assertion wasDerivedFrom befree-20150227 NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_provenance.
- NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_assertion wasGeneratedBy ECO_0000203 NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_provenance.