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- source_evidence_literature type ECO_0000212 NP1266377.RA-gkzBJNXNaXLGZ7f7bgIdjZG3NYMdZeOsToC9CNTHeg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1266377.RA-gkzBJNXNaXLGZ7f7bgIdjZG3NYMdZeOsToC9CNTHeg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1266377.RA-gkzBJNXNaXLGZ7f7bgIdjZG3NYMdZeOsToC9CNTHeg130_provenance.
- NP1266377.RA-gkzBJNXNaXLGZ7f7bgIdjZG3NYMdZeOsToC9CNTHeg130_assertion description "[We screened 9 genotype-negative probands with sick sinus syndrome families for mutations in MYH6 and identified an in-frame 3-bp deletion predicted to delete one residue (delE933) at the highly conserved coiled-coil structure within the binding motif to myosin-binding protein C in one patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266377.RA-gkzBJNXNaXLGZ7f7bgIdjZG3NYMdZeOsToC9CNTHeg130_provenance.
- NP1266377.RA-gkzBJNXNaXLGZ7f7bgIdjZG3NYMdZeOsToC9CNTHeg130_assertion evidence source_evidence_literature NP1266377.RA-gkzBJNXNaXLGZ7f7bgIdjZG3NYMdZeOsToC9CNTHeg130_provenance.
- NP1266377.RA-gkzBJNXNaXLGZ7f7bgIdjZG3NYMdZeOsToC9CNTHeg130_assertion SIO_000772 25717017 NP1266377.RA-gkzBJNXNaXLGZ7f7bgIdjZG3NYMdZeOsToC9CNTHeg130_provenance.
- NP1266377.RA-gkzBJNXNaXLGZ7f7bgIdjZG3NYMdZeOsToC9CNTHeg130_assertion wasDerivedFrom befree-2016 NP1266377.RA-gkzBJNXNaXLGZ7f7bgIdjZG3NYMdZeOsToC9CNTHeg130_provenance.
- NP1266377.RA-gkzBJNXNaXLGZ7f7bgIdjZG3NYMdZeOsToC9CNTHeg130_assertion wasGeneratedBy ECO_0000203 NP1266377.RA-gkzBJNXNaXLGZ7f7bgIdjZG3NYMdZeOsToC9CNTHeg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1266377.RA-gkzBJNXNaXLGZ7f7bgIdjZG3NYMdZeOsToC9CNTHeg130_provenance.