Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7550.RA7GVQwq45QA0T12uNKCvQKGFQR8TpQo_ggLzjGTmY5ZA130_assertion> ?p ?o ?g. }
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- NP7550.RA7GVQwq45QA0T12uNKCvQKGFQR8TpQo_ggLzjGTmY5ZA130_assertion type Assertion NP7550.RA7GVQwq45QA0T12uNKCvQKGFQR8TpQo_ggLzjGTmY5ZA130_head.
- NP7550.RA7GVQwq45QA0T12uNKCvQKGFQR8TpQo_ggLzjGTmY5ZA130_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." NP7550.RA7GVQwq45QA0T12uNKCvQKGFQR8TpQo_ggLzjGTmY5ZA130_provenance.
- NP7550.RA7GVQwq45QA0T12uNKCvQKGFQR8TpQo_ggLzjGTmY5ZA130_assertion evidence source_evidence_curated NP7550.RA7GVQwq45QA0T12uNKCvQKGFQR8TpQo_ggLzjGTmY5ZA130_provenance.
- NP7550.RA7GVQwq45QA0T12uNKCvQKGFQR8TpQo_ggLzjGTmY5ZA130_assertion SIO_000772 23768516 NP7550.RA7GVQwq45QA0T12uNKCvQKGFQR8TpQo_ggLzjGTmY5ZA130_provenance.
- NP7550.RA7GVQwq45QA0T12uNKCvQKGFQR8TpQo_ggLzjGTmY5ZA130_assertion wasDerivedFrom uniprot-2016 NP7550.RA7GVQwq45QA0T12uNKCvQKGFQR8TpQo_ggLzjGTmY5ZA130_provenance.
- NP7550.RA7GVQwq45QA0T12uNKCvQKGFQR8TpQo_ggLzjGTmY5ZA130_assertion wasGeneratedBy ECO_0000218 NP7550.RA7GVQwq45QA0T12uNKCvQKGFQR8TpQo_ggLzjGTmY5ZA130_provenance.