Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP967729.RAGJAO2kV7zwe0iwtj2h6w9Yoz4ICDUqCzASKdHV89Ea4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP967729.RAGJAO2kV7zwe0iwtj2h6w9Yoz4ICDUqCzASKdHV89Ea4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP967729.RAGJAO2kV7zwe0iwtj2h6w9Yoz4ICDUqCzASKdHV89Ea4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP967729.RAGJAO2kV7zwe0iwtj2h6w9Yoz4ICDUqCzASKdHV89Ea4130_provenance.
- NP967729.RAGJAO2kV7zwe0iwtj2h6w9Yoz4ICDUqCzASKdHV89Ea4130_assertion description "[Mutations in RYR1 are associated with several congenital myopathies (termed RYR1-related myopathies) that are the most common non-dystrophic muscle diseases of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP967729.RAGJAO2kV7zwe0iwtj2h6w9Yoz4ICDUqCzASKdHV89Ea4130_provenance.
- NP967729.RAGJAO2kV7zwe0iwtj2h6w9Yoz4ICDUqCzASKdHV89Ea4130_assertion evidence source_evidence_literature NP967729.RAGJAO2kV7zwe0iwtj2h6w9Yoz4ICDUqCzASKdHV89Ea4130_provenance.
- NP967729.RAGJAO2kV7zwe0iwtj2h6w9Yoz4ICDUqCzASKdHV89Ea4130_assertion SIO_000772 22418739 NP967729.RAGJAO2kV7zwe0iwtj2h6w9Yoz4ICDUqCzASKdHV89Ea4130_provenance.
- NP967729.RAGJAO2kV7zwe0iwtj2h6w9Yoz4ICDUqCzASKdHV89Ea4130_assertion wasDerivedFrom befree-2016 NP967729.RAGJAO2kV7zwe0iwtj2h6w9Yoz4ICDUqCzASKdHV89Ea4130_provenance.
- NP967729.RAGJAO2kV7zwe0iwtj2h6w9Yoz4ICDUqCzASKdHV89Ea4130_assertion wasGeneratedBy ECO_0000203 NP967729.RAGJAO2kV7zwe0iwtj2h6w9Yoz4ICDUqCzASKdHV89Ea4130_provenance.
- befree-2016 importedOn "2016-02-19" NP967729.RAGJAO2kV7zwe0iwtj2h6w9Yoz4ICDUqCzASKdHV89Ea4130_provenance.