Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP542121.RA-qP6R00SXKje-3hvvvlxsegRLDF1CUfY1AWMJvjYCtI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP542121.RA-qP6R00SXKje-3hvvvlxsegRLDF1CUfY1AWMJvjYCtI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP542121.RA-qP6R00SXKje-3hvvvlxsegRLDF1CUfY1AWMJvjYCtI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP542121.RA-qP6R00SXKje-3hvvvlxsegRLDF1CUfY1AWMJvjYCtI130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP542121.RA-qP6R00SXKje-3hvvvlxsegRLDF1CUfY1AWMJvjYCtI130_provenance.