Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP618714.RAOaaXp_44VWnQCkYr6a9zB2obCr9gGxilhNRrTYBrURM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP618714.RAOaaXp_44VWnQCkYr6a9zB2obCr9gGxilhNRrTYBrURM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP618714.RAOaaXp_44VWnQCkYr6a9zB2obCr9gGxilhNRrTYBrURM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP618714.RAOaaXp_44VWnQCkYr6a9zB2obCr9gGxilhNRrTYBrURM130_provenance.
- NP618714.RAOaaXp_44VWnQCkYr6a9zB2obCr9gGxilhNRrTYBrURM130_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." NP618714.RAOaaXp_44VWnQCkYr6a9zB2obCr9gGxilhNRrTYBrURM130_provenance.
- NP618714.RAOaaXp_44VWnQCkYr6a9zB2obCr9gGxilhNRrTYBrURM130_assertion evidence source_evidence_literature NP618714.RAOaaXp_44VWnQCkYr6a9zB2obCr9gGxilhNRrTYBrURM130_provenance.
- NP618714.RAOaaXp_44VWnQCkYr6a9zB2obCr9gGxilhNRrTYBrURM130_assertion SIO_000772 17612745 NP618714.RAOaaXp_44VWnQCkYr6a9zB2obCr9gGxilhNRrTYBrURM130_provenance.
- NP618714.RAOaaXp_44VWnQCkYr6a9zB2obCr9gGxilhNRrTYBrURM130_assertion wasDerivedFrom befree-2016 NP618714.RAOaaXp_44VWnQCkYr6a9zB2obCr9gGxilhNRrTYBrURM130_provenance.
- NP618714.RAOaaXp_44VWnQCkYr6a9zB2obCr9gGxilhNRrTYBrURM130_assertion wasGeneratedBy ECO_0000203 NP618714.RAOaaXp_44VWnQCkYr6a9zB2obCr9gGxilhNRrTYBrURM130_provenance.
- befree-2016 importedOn "2016-02-19" NP618714.RAOaaXp_44VWnQCkYr6a9zB2obCr9gGxilhNRrTYBrURM130_provenance.