Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP458496.RAMpgC8O8NWjXgoxDnAnZvnqtZtqdA2osyhGjjPgKb8zg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP458496.RAMpgC8O8NWjXgoxDnAnZvnqtZtqdA2osyhGjjPgKb8zg130_assertion type Assertion NP458496.RAMpgC8O8NWjXgoxDnAnZvnqtZtqdA2osyhGjjPgKb8zg130_head.
- NP458496.RAMpgC8O8NWjXgoxDnAnZvnqtZtqdA2osyhGjjPgKb8zg130_assertion description "[In this study we analyzed the genotype and phenotype of individuals from two unrelated families with HCM in which the affected individuals have the same missense mutation in exon 13 (G1208A) of the coding sequence for beta MHC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP458496.RAMpgC8O8NWjXgoxDnAnZvnqtZtqdA2osyhGjjPgKb8zg130_provenance.
- NP458496.RAMpgC8O8NWjXgoxDnAnZvnqtZtqdA2osyhGjjPgKb8zg130_assertion evidence source_evidence_literature NP458496.RAMpgC8O8NWjXgoxDnAnZvnqtZtqdA2osyhGjjPgKb8zg130_provenance.
- NP458496.RAMpgC8O8NWjXgoxDnAnZvnqtZtqdA2osyhGjjPgKb8zg130_assertion SIO_000772 7934006 NP458496.RAMpgC8O8NWjXgoxDnAnZvnqtZtqdA2osyhGjjPgKb8zg130_provenance.
- NP458496.RAMpgC8O8NWjXgoxDnAnZvnqtZtqdA2osyhGjjPgKb8zg130_assertion wasDerivedFrom befree-20150227 NP458496.RAMpgC8O8NWjXgoxDnAnZvnqtZtqdA2osyhGjjPgKb8zg130_provenance.
- NP458496.RAMpgC8O8NWjXgoxDnAnZvnqtZtqdA2osyhGjjPgKb8zg130_assertion wasGeneratedBy ECO_0000203 NP458496.RAMpgC8O8NWjXgoxDnAnZvnqtZtqdA2osyhGjjPgKb8zg130_provenance.