Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP542119.RAIomxDYXj9cfNd3IOpeawvP_72OIecneYYjKqqzzlevM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP542119.RAIomxDYXj9cfNd3IOpeawvP_72OIecneYYjKqqzzlevM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP542119.RAIomxDYXj9cfNd3IOpeawvP_72OIecneYYjKqqzzlevM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP542119.RAIomxDYXj9cfNd3IOpeawvP_72OIecneYYjKqqzzlevM130_provenance.
- NP542119.RAIomxDYXj9cfNd3IOpeawvP_72OIecneYYjKqqzzlevM130_assertion description "[In a Portuguese population of 45 HCM patients, 5 (11.1%) had mutations in the MYBPC3 gene (3 missense mutations--theoretically less frequent in the MYBPC3 gene--and 2 deletions).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP542119.RAIomxDYXj9cfNd3IOpeawvP_72OIecneYYjKqqzzlevM130_provenance.
- NP542119.RAIomxDYXj9cfNd3IOpeawvP_72OIecneYYjKqqzzlevM130_assertion evidence source_evidence_literature NP542119.RAIomxDYXj9cfNd3IOpeawvP_72OIecneYYjKqqzzlevM130_provenance.
- NP542119.RAIomxDYXj9cfNd3IOpeawvP_72OIecneYYjKqqzzlevM130_assertion SIO_000772 16566405 NP542119.RAIomxDYXj9cfNd3IOpeawvP_72OIecneYYjKqqzzlevM130_provenance.
- NP542119.RAIomxDYXj9cfNd3IOpeawvP_72OIecneYYjKqqzzlevM130_assertion wasDerivedFrom befree-2016 NP542119.RAIomxDYXj9cfNd3IOpeawvP_72OIecneYYjKqqzzlevM130_provenance.
- NP542119.RAIomxDYXj9cfNd3IOpeawvP_72OIecneYYjKqqzzlevM130_assertion wasGeneratedBy ECO_0000203 NP542119.RAIomxDYXj9cfNd3IOpeawvP_72OIecneYYjKqqzzlevM130_provenance.
- befree-2016 importedOn "2016-02-19" NP542119.RAIomxDYXj9cfNd3IOpeawvP_72OIecneYYjKqqzzlevM130_provenance.