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- source_evidence_literature type ECO_0000212 NP748684.RA06OBoDmvIYWo9m1CT3rQBKhuNOlLfBG2pbta-M1yzXA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP748684.RA06OBoDmvIYWo9m1CT3rQBKhuNOlLfBG2pbta-M1yzXA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP748684.RA06OBoDmvIYWo9m1CT3rQBKhuNOlLfBG2pbta-M1yzXA130_provenance.
- NP748684.RA06OBoDmvIYWo9m1CT3rQBKhuNOlLfBG2pbta-M1yzXA130_assertion description "[We previously described cross-sectional family studies of two hypertrophic cardiomyopathy (HCM)-causing mutations, R92W(TNNT2) and R403W(MYH7), both associated with minimal hypertrophy, but with widely different life expectancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748684.RA06OBoDmvIYWo9m1CT3rQBKhuNOlLfBG2pbta-M1yzXA130_provenance.
- NP748684.RA06OBoDmvIYWo9m1CT3rQBKhuNOlLfBG2pbta-M1yzXA130_assertion evidence source_evidence_literature NP748684.RA06OBoDmvIYWo9m1CT3rQBKhuNOlLfBG2pbta-M1yzXA130_provenance.
- NP748684.RA06OBoDmvIYWo9m1CT3rQBKhuNOlLfBG2pbta-M1yzXA130_assertion SIO_000772 17612745 NP748684.RA06OBoDmvIYWo9m1CT3rQBKhuNOlLfBG2pbta-M1yzXA130_provenance.
- NP748684.RA06OBoDmvIYWo9m1CT3rQBKhuNOlLfBG2pbta-M1yzXA130_assertion wasDerivedFrom befree-20150227 NP748684.RA06OBoDmvIYWo9m1CT3rQBKhuNOlLfBG2pbta-M1yzXA130_provenance.
- NP748684.RA06OBoDmvIYWo9m1CT3rQBKhuNOlLfBG2pbta-M1yzXA130_assertion wasGeneratedBy ECO_0000203 NP748684.RA06OBoDmvIYWo9m1CT3rQBKhuNOlLfBG2pbta-M1yzXA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP748684.RA06OBoDmvIYWo9m1CT3rQBKhuNOlLfBG2pbta-M1yzXA130_provenance.