Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP542121.RA-qP6R00SXKje-3hvvvlxsegRLDF1CUfY1AWMJvjYCtI130_assertion> ?p ?o ?g. }
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- NP542121.RA-qP6R00SXKje-3hvvvlxsegRLDF1CUfY1AWMJvjYCtI130_assertion type Assertion NP542121.RA-qP6R00SXKje-3hvvvlxsegRLDF1CUfY1AWMJvjYCtI130_head.
- NP542121.RA-qP6R00SXKje-3hvvvlxsegRLDF1CUfY1AWMJvjYCtI130_assertion description "[Of the 45 patients, 5 (11.1%) showed mutations in the MYBPC3 gene (2 deletions and 3 missense mutations), all in patients with familial HCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP542121.RA-qP6R00SXKje-3hvvvlxsegRLDF1CUfY1AWMJvjYCtI130_provenance.
- NP542121.RA-qP6R00SXKje-3hvvvlxsegRLDF1CUfY1AWMJvjYCtI130_assertion evidence source_evidence_literature NP542121.RA-qP6R00SXKje-3hvvvlxsegRLDF1CUfY1AWMJvjYCtI130_provenance.
- NP542121.RA-qP6R00SXKje-3hvvvlxsegRLDF1CUfY1AWMJvjYCtI130_assertion SIO_000772 16566405 NP542121.RA-qP6R00SXKje-3hvvvlxsegRLDF1CUfY1AWMJvjYCtI130_provenance.
- NP542121.RA-qP6R00SXKje-3hvvvlxsegRLDF1CUfY1AWMJvjYCtI130_assertion wasDerivedFrom befree-2016 NP542121.RA-qP6R00SXKje-3hvvvlxsegRLDF1CUfY1AWMJvjYCtI130_provenance.
- NP542121.RA-qP6R00SXKje-3hvvvlxsegRLDF1CUfY1AWMJvjYCtI130_assertion wasGeneratedBy ECO_0000203 NP542121.RA-qP6R00SXKje-3hvvvlxsegRLDF1CUfY1AWMJvjYCtI130_provenance.