Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP96174.RAjv90u7ENHerkzwqoXO8mjhNa9bbmJHoFEsp96W4uWTE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP96174.RAjv90u7ENHerkzwqoXO8mjhNa9bbmJHoFEsp96W4uWTE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP96174.RAjv90u7ENHerkzwqoXO8mjhNa9bbmJHoFEsp96W4uWTE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP96174.RAjv90u7ENHerkzwqoXO8mjhNa9bbmJHoFEsp96W4uWTE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP96174.RAjv90u7ENHerkzwqoXO8mjhNa9bbmJHoFEsp96W4uWTE130_provenance.
- NP96174.RAjv90u7ENHerkzwqoXO8mjhNa9bbmJHoFEsp96W4uWTE130_assertion wasGeneratedBy ECO_0000203 NP96174.RAjv90u7ENHerkzwqoXO8mjhNa9bbmJHoFEsp96W4uWTE130_provenance.
- NP96174.RAjv90u7ENHerkzwqoXO8mjhNa9bbmJHoFEsp96W4uWTE130_assertion wasDerivedFrom gad-20150221 NP96174.RAjv90u7ENHerkzwqoXO8mjhNa9bbmJHoFEsp96W4uWTE130_provenance.
- NP96174.RAjv90u7ENHerkzwqoXO8mjhNa9bbmJHoFEsp96W4uWTE130_assertion SIO_000772 16199542 NP96174.RAjv90u7ENHerkzwqoXO8mjhNa9bbmJHoFEsp96W4uWTE130_provenance.
- NP96174.RAjv90u7ENHerkzwqoXO8mjhNa9bbmJHoFEsp96W4uWTE130_assertion evidence source_evidence_literature NP96174.RAjv90u7ENHerkzwqoXO8mjhNa9bbmJHoFEsp96W4uWTE130_provenance.
- NP96174.RAjv90u7ENHerkzwqoXO8mjhNa9bbmJHoFEsp96W4uWTE130_assertion description "[ Multiple gene mutations occurring in HCM families may result in a more severe clinical phenotype because of a double dose effect. This highlights the importance of screening the entire panel of HCM genes even after a single mutation has been identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96174.RAjv90u7ENHerkzwqoXO8mjhNa9bbmJHoFEsp96W4uWTE130_provenance.