Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP82095.RAA2HSwoyGF7A1PgBnWXub0MjDbWvTkJZ_a-askDk7cOU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP82095.RAA2HSwoyGF7A1PgBnWXub0MjDbWvTkJZ_a-askDk7cOU130_assertion type Assertion NP82095.RAA2HSwoyGF7A1PgBnWXub0MjDbWvTkJZ_a-askDk7cOU130_head.
- NP82095.RAA2HSwoyGF7A1PgBnWXub0MjDbWvTkJZ_a-askDk7cOU130_assertion description "[This study shows that familial disease is common among infants and children with HCM and that, in most cases, disease is caused by mutations in cardiac sarcomere protein genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82095.RAA2HSwoyGF7A1PgBnWXub0MjDbWvTkJZ_a-askDk7cOU130_provenance.
- NP82095.RAA2HSwoyGF7A1PgBnWXub0MjDbWvTkJZ_a-askDk7cOU130_assertion evidence source_evidence_literature NP82095.RAA2HSwoyGF7A1PgBnWXub0MjDbWvTkJZ_a-askDk7cOU130_provenance.
- NP82095.RAA2HSwoyGF7A1PgBnWXub0MjDbWvTkJZ_a-askDk7cOU130_assertion SIO_000772 20031618 NP82095.RAA2HSwoyGF7A1PgBnWXub0MjDbWvTkJZ_a-askDk7cOU130_provenance.
- NP82095.RAA2HSwoyGF7A1PgBnWXub0MjDbWvTkJZ_a-askDk7cOU130_assertion wasDerivedFrom gad-20130706 NP82095.RAA2HSwoyGF7A1PgBnWXub0MjDbWvTkJZ_a-askDk7cOU130_provenance.
- NP82095.RAA2HSwoyGF7A1PgBnWXub0MjDbWvTkJZ_a-askDk7cOU130_assertion wasGeneratedBy ECO_0000203 NP82095.RAA2HSwoyGF7A1PgBnWXub0MjDbWvTkJZ_a-askDk7cOU130_provenance.