Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1175827.RAQPq1Ebyfl-iL-Lhu4cYGVRaMfXOgx9ooxg0s0zPR3cM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1175827.RAQPq1Ebyfl-iL-Lhu4cYGVRaMfXOgx9ooxg0s0zPR3cM130_assertion type Assertion NP1175827.RAQPq1Ebyfl-iL-Lhu4cYGVRaMfXOgx9ooxg0s0zPR3cM130_head.
- NP1175827.RAQPq1Ebyfl-iL-Lhu4cYGVRaMfXOgx9ooxg0s0zPR3cM130_assertion description "[Identification of two novel SMCHD1 sequence variants in families with FSHD-like muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1175827.RAQPq1Ebyfl-iL-Lhu4cYGVRaMfXOgx9ooxg0s0zPR3cM130_provenance.
- NP1175827.RAQPq1Ebyfl-iL-Lhu4cYGVRaMfXOgx9ooxg0s0zPR3cM130_assertion evidence source_evidence_literature NP1175827.RAQPq1Ebyfl-iL-Lhu4cYGVRaMfXOgx9ooxg0s0zPR3cM130_provenance.
- NP1175827.RAQPq1Ebyfl-iL-Lhu4cYGVRaMfXOgx9ooxg0s0zPR3cM130_assertion SIO_000772 24755953 NP1175827.RAQPq1Ebyfl-iL-Lhu4cYGVRaMfXOgx9ooxg0s0zPR3cM130_provenance.
- NP1175827.RAQPq1Ebyfl-iL-Lhu4cYGVRaMfXOgx9ooxg0s0zPR3cM130_assertion wasDerivedFrom befree-2016 NP1175827.RAQPq1Ebyfl-iL-Lhu4cYGVRaMfXOgx9ooxg0s0zPR3cM130_provenance.
- NP1175827.RAQPq1Ebyfl-iL-Lhu4cYGVRaMfXOgx9ooxg0s0zPR3cM130_assertion wasGeneratedBy ECO_0000203 NP1175827.RAQPq1Ebyfl-iL-Lhu4cYGVRaMfXOgx9ooxg0s0zPR3cM130_provenance.