Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP924690.RAP6Ufxqwa2oNCeVCb9KxHnx2ULFADbYBRJLtNqJOpWmQ130_assertion> ?p ?o ?g. }
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- NP924690.RAP6Ufxqwa2oNCeVCb9KxHnx2ULFADbYBRJLtNqJOpWmQ130_assertion type Assertion NP924690.RAP6Ufxqwa2oNCeVCb9KxHnx2ULFADbYBRJLtNqJOpWmQ130_head.
- NP924690.RAP6Ufxqwa2oNCeVCb9KxHnx2ULFADbYBRJLtNqJOpWmQ130_assertion description "[Since the creatine transporter has a prominent function in muscular physiology, it is a candidate gene for Barth syndrome and infantile cardiomyopathy mapped to Xq28.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924690.RAP6Ufxqwa2oNCeVCb9KxHnx2ULFADbYBRJLtNqJOpWmQ130_provenance.
- NP924690.RAP6Ufxqwa2oNCeVCb9KxHnx2ULFADbYBRJLtNqJOpWmQ130_assertion evidence source_evidence_literature NP924690.RAP6Ufxqwa2oNCeVCb9KxHnx2ULFADbYBRJLtNqJOpWmQ130_provenance.
- NP924690.RAP6Ufxqwa2oNCeVCb9KxHnx2ULFADbYBRJLtNqJOpWmQ130_assertion SIO_000772 8661155 NP924690.RAP6Ufxqwa2oNCeVCb9KxHnx2ULFADbYBRJLtNqJOpWmQ130_provenance.
- NP924690.RAP6Ufxqwa2oNCeVCb9KxHnx2ULFADbYBRJLtNqJOpWmQ130_assertion wasDerivedFrom befree-20140225 NP924690.RAP6Ufxqwa2oNCeVCb9KxHnx2ULFADbYBRJLtNqJOpWmQ130_provenance.
- NP924690.RAP6Ufxqwa2oNCeVCb9KxHnx2ULFADbYBRJLtNqJOpWmQ130_assertion wasGeneratedBy ECO_0000203 NP924690.RAP6Ufxqwa2oNCeVCb9KxHnx2ULFADbYBRJLtNqJOpWmQ130_provenance.