Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1086059.RAJ5vL1MPei1DVBJKmGMDGd5W1mwNKzg3NumKEe4LrXjA130_assertion> ?p ?o ?g. }
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- NP1086059.RAJ5vL1MPei1DVBJKmGMDGd5W1mwNKzg3NumKEe4LrXjA130_assertion type Assertion NP1086059.RAJ5vL1MPei1DVBJKmGMDGd5W1mwNKzg3NumKEe4LrXjA130_head.
- NP1086059.RAJ5vL1MPei1DVBJKmGMDGd5W1mwNKzg3NumKEe4LrXjA130_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." NP1086059.RAJ5vL1MPei1DVBJKmGMDGd5W1mwNKzg3NumKEe4LrXjA130_provenance.
- NP1086059.RAJ5vL1MPei1DVBJKmGMDGd5W1mwNKzg3NumKEe4LrXjA130_assertion evidence source_evidence_literature NP1086059.RAJ5vL1MPei1DVBJKmGMDGd5W1mwNKzg3NumKEe4LrXjA130_provenance.
- NP1086059.RAJ5vL1MPei1DVBJKmGMDGd5W1mwNKzg3NumKEe4LrXjA130_assertion SIO_000772 23768516 NP1086059.RAJ5vL1MPei1DVBJKmGMDGd5W1mwNKzg3NumKEe4LrXjA130_provenance.
- NP1086059.RAJ5vL1MPei1DVBJKmGMDGd5W1mwNKzg3NumKEe4LrXjA130_assertion wasDerivedFrom befree-2016 NP1086059.RAJ5vL1MPei1DVBJKmGMDGd5W1mwNKzg3NumKEe4LrXjA130_provenance.
- NP1086059.RAJ5vL1MPei1DVBJKmGMDGd5W1mwNKzg3NumKEe4LrXjA130_assertion wasGeneratedBy ECO_0000203 NP1086059.RAJ5vL1MPei1DVBJKmGMDGd5W1mwNKzg3NumKEe4LrXjA130_provenance.