Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP4307.RAK5AQ2dEG96Oa4XaAGBOFnbQEjVCGY8nOgiRh3mrCMtU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP4307.RAK5AQ2dEG96Oa4XaAGBOFnbQEjVCGY8nOgiRh3mrCMtU130_assertion type Assertion NP4307.RAK5AQ2dEG96Oa4XaAGBOFnbQEjVCGY8nOgiRh3mrCMtU130_head.
- NP4307.RAK5AQ2dEG96Oa4XaAGBOFnbQEjVCGY8nOgiRh3mrCMtU130_assertion description "[Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4307.RAK5AQ2dEG96Oa4XaAGBOFnbQEjVCGY8nOgiRh3mrCMtU130_provenance.
- NP4307.RAK5AQ2dEG96Oa4XaAGBOFnbQEjVCGY8nOgiRh3mrCMtU130_assertion evidence source_evidence_curated NP4307.RAK5AQ2dEG96Oa4XaAGBOFnbQEjVCGY8nOgiRh3mrCMtU130_provenance.
- NP4307.RAK5AQ2dEG96Oa4XaAGBOFnbQEjVCGY8nOgiRh3mrCMtU130_assertion SIO_000772 10973259 NP4307.RAK5AQ2dEG96Oa4XaAGBOFnbQEjVCGY8nOgiRh3mrCMtU130_provenance.
- NP4307.RAK5AQ2dEG96Oa4XaAGBOFnbQEjVCGY8nOgiRh3mrCMtU130_assertion wasDerivedFrom uniprot-20130724 NP4307.RAK5AQ2dEG96Oa4XaAGBOFnbQEjVCGY8nOgiRh3mrCMtU130_provenance.
- NP4307.RAK5AQ2dEG96Oa4XaAGBOFnbQEjVCGY8nOgiRh3mrCMtU130_assertion wasGeneratedBy ECO_0000218 NP4307.RAK5AQ2dEG96Oa4XaAGBOFnbQEjVCGY8nOgiRh3mrCMtU130_provenance.