Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1266123.RAuDXBjhWLTCvY-sqkUkTDjDHTDZyS4jK0Rvqd9LVuYFM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1266123.RAuDXBjhWLTCvY-sqkUkTDjDHTDZyS4jK0Rvqd9LVuYFM130_assertion type Assertion NP1266123.RAuDXBjhWLTCvY-sqkUkTDjDHTDZyS4jK0Rvqd9LVuYFM130_head.
- NP1266123.RAuDXBjhWLTCvY-sqkUkTDjDHTDZyS4jK0Rvqd9LVuYFM130_assertion description "[The involvement of congenital anomalies in all 16 clinically described patients with EP300 mutations (25% of which have been identified by hypothesis free methods, including microarray, exome, and whole-genome sequencing) is reviewed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266123.RAuDXBjhWLTCvY-sqkUkTDjDHTDZyS4jK0Rvqd9LVuYFM130_provenance.
- NP1266123.RAuDXBjhWLTCvY-sqkUkTDjDHTDZyS4jK0Rvqd9LVuYFM130_assertion evidence source_evidence_literature NP1266123.RAuDXBjhWLTCvY-sqkUkTDjDHTDZyS4jK0Rvqd9LVuYFM130_provenance.
- NP1266123.RAuDXBjhWLTCvY-sqkUkTDjDHTDZyS4jK0Rvqd9LVuYFM130_assertion SIO_000772 25712426 NP1266123.RAuDXBjhWLTCvY-sqkUkTDjDHTDZyS4jK0Rvqd9LVuYFM130_provenance.
- NP1266123.RAuDXBjhWLTCvY-sqkUkTDjDHTDZyS4jK0Rvqd9LVuYFM130_assertion wasDerivedFrom befree-2016 NP1266123.RAuDXBjhWLTCvY-sqkUkTDjDHTDZyS4jK0Rvqd9LVuYFM130_provenance.
- NP1266123.RAuDXBjhWLTCvY-sqkUkTDjDHTDZyS4jK0Rvqd9LVuYFM130_assertion wasGeneratedBy ECO_0000203 NP1266123.RAuDXBjhWLTCvY-sqkUkTDjDHTDZyS4jK0Rvqd9LVuYFM130_provenance.