Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP670055.RAZW2O8ETfnqUeTFJgq7aTmmeKrkicylVaTQ0xu6eW60o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP670055.RAZW2O8ETfnqUeTFJgq7aTmmeKrkicylVaTQ0xu6eW60o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP670055.RAZW2O8ETfnqUeTFJgq7aTmmeKrkicylVaTQ0xu6eW60o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP670055.RAZW2O8ETfnqUeTFJgq7aTmmeKrkicylVaTQ0xu6eW60o130_provenance.
- NP670055.RAZW2O8ETfnqUeTFJgq7aTmmeKrkicylVaTQ0xu6eW60o130_assertion description "[Homozygous mutations in the MYBPC3 gene have been identified as the cause of severe infantile HCM among the Amish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670055.RAZW2O8ETfnqUeTFJgq7aTmmeKrkicylVaTQ0xu6eW60o130_provenance.
- NP670055.RAZW2O8ETfnqUeTFJgq7aTmmeKrkicylVaTQ0xu6eW60o130_assertion evidence source_evidence_literature NP670055.RAZW2O8ETfnqUeTFJgq7aTmmeKrkicylVaTQ0xu6eW60o130_provenance.
- NP670055.RAZW2O8ETfnqUeTFJgq7aTmmeKrkicylVaTQ0xu6eW60o130_assertion SIO_000772 18467358 NP670055.RAZW2O8ETfnqUeTFJgq7aTmmeKrkicylVaTQ0xu6eW60o130_provenance.
- NP670055.RAZW2O8ETfnqUeTFJgq7aTmmeKrkicylVaTQ0xu6eW60o130_assertion wasDerivedFrom befree-2016 NP670055.RAZW2O8ETfnqUeTFJgq7aTmmeKrkicylVaTQ0xu6eW60o130_provenance.
- NP670055.RAZW2O8ETfnqUeTFJgq7aTmmeKrkicylVaTQ0xu6eW60o130_assertion wasGeneratedBy ECO_0000203 NP670055.RAZW2O8ETfnqUeTFJgq7aTmmeKrkicylVaTQ0xu6eW60o130_provenance.
- befree-2016 importedOn "2016-02-19" NP670055.RAZW2O8ETfnqUeTFJgq7aTmmeKrkicylVaTQ0xu6eW60o130_provenance.