Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_assertion> ?p ?o ?g. }
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- NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_assertion type Assertion NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_head.
- NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_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." NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_provenance.
- NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_assertion evidence source_evidence_literature NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_provenance.
- NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_assertion SIO_000772 23768516 NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_provenance.
- NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_assertion wasDerivedFrom befree-20150227 NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_provenance.
- NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_assertion wasGeneratedBy ECO_0000203 NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_provenance.