Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1044832.RA6sjjIRPY_J4vjSAbnvDDYEJMSPuDU9AIz4sTNO34HfM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1044832.RA6sjjIRPY_J4vjSAbnvDDYEJMSPuDU9AIz4sTNO34HfM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1044832.RA6sjjIRPY_J4vjSAbnvDDYEJMSPuDU9AIz4sTNO34HfM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1044832.RA6sjjIRPY_J4vjSAbnvDDYEJMSPuDU9AIz4sTNO34HfM130_provenance.
- NP1044832.RA6sjjIRPY_J4vjSAbnvDDYEJMSPuDU9AIz4sTNO34HfM130_assertion description "[A novel late-onset axial myopathy associated with mutations in the skeletal muscle ryanodine receptor (RYR1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1044832.RA6sjjIRPY_J4vjSAbnvDDYEJMSPuDU9AIz4sTNO34HfM130_provenance.
- NP1044832.RA6sjjIRPY_J4vjSAbnvDDYEJMSPuDU9AIz4sTNO34HfM130_assertion evidence source_evidence_literature NP1044832.RA6sjjIRPY_J4vjSAbnvDDYEJMSPuDU9AIz4sTNO34HfM130_provenance.
- NP1044832.RA6sjjIRPY_J4vjSAbnvDDYEJMSPuDU9AIz4sTNO34HfM130_assertion SIO_000772 23329375 NP1044832.RA6sjjIRPY_J4vjSAbnvDDYEJMSPuDU9AIz4sTNO34HfM130_provenance.
- NP1044832.RA6sjjIRPY_J4vjSAbnvDDYEJMSPuDU9AIz4sTNO34HfM130_assertion wasDerivedFrom befree-2016 NP1044832.RA6sjjIRPY_J4vjSAbnvDDYEJMSPuDU9AIz4sTNO34HfM130_provenance.
- NP1044832.RA6sjjIRPY_J4vjSAbnvDDYEJMSPuDU9AIz4sTNO34HfM130_assertion wasGeneratedBy ECO_0000203 NP1044832.RA6sjjIRPY_J4vjSAbnvDDYEJMSPuDU9AIz4sTNO34HfM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1044832.RA6sjjIRPY_J4vjSAbnvDDYEJMSPuDU9AIz4sTNO34HfM130_provenance.