Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP898396.RABTDjg5O-IHXSr6SqalG0zeTTyNEfJ9veFBZcMXiONko130_assertion> ?p ?o ?g. }
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- NP898396.RABTDjg5O-IHXSr6SqalG0zeTTyNEfJ9veFBZcMXiONko130_assertion type Assertion NP898396.RABTDjg5O-IHXSr6SqalG0zeTTyNEfJ9veFBZcMXiONko130_head.
- NP898396.RABTDjg5O-IHXSr6SqalG0zeTTyNEfJ9veFBZcMXiONko130_assertion description "[For instance, identification of MYH9 as the gene whose mutations cause the May-Hegglin anomaly led to the recognition that Sebastian platelet syndrome, Epstein syndrome, and Fechtner syndrome derive from mutations of the same gene and describe overlapping disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP898396.RABTDjg5O-IHXSr6SqalG0zeTTyNEfJ9veFBZcMXiONko130_provenance.
- NP898396.RABTDjg5O-IHXSr6SqalG0zeTTyNEfJ9veFBZcMXiONko130_assertion evidence source_evidence_literature NP898396.RABTDjg5O-IHXSr6SqalG0zeTTyNEfJ9veFBZcMXiONko130_provenance.
- NP898396.RABTDjg5O-IHXSr6SqalG0zeTTyNEfJ9veFBZcMXiONko130_assertion SIO_000772 22886561 NP898396.RABTDjg5O-IHXSr6SqalG0zeTTyNEfJ9veFBZcMXiONko130_provenance.
- NP898396.RABTDjg5O-IHXSr6SqalG0zeTTyNEfJ9veFBZcMXiONko130_assertion wasDerivedFrom befree-20140225 NP898396.RABTDjg5O-IHXSr6SqalG0zeTTyNEfJ9veFBZcMXiONko130_provenance.
- NP898396.RABTDjg5O-IHXSr6SqalG0zeTTyNEfJ9veFBZcMXiONko130_assertion wasGeneratedBy ECO_0000203 NP898396.RABTDjg5O-IHXSr6SqalG0zeTTyNEfJ9veFBZcMXiONko130_provenance.