Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP652033.RAVmTp_naw9AGjeStP4RkFZCkK6fru2EasqPNlW6xNMAY130_assertion> ?p ?o ?g. }
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- NP652033.RAVmTp_naw9AGjeStP4RkFZCkK6fru2EasqPNlW6xNMAY130_assertion type Assertion NP652033.RAVmTp_naw9AGjeStP4RkFZCkK6fru2EasqPNlW6xNMAY130_head.
- NP652033.RAVmTp_naw9AGjeStP4RkFZCkK6fru2EasqPNlW6xNMAY130_assertion description "[These results show that secondary changes in the expression of dystrophin can occur in the absence of an abnormality in the corresponding gene and that dystrophin cannot be used in isolation as a diagnostic marker for muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP652033.RAVmTp_naw9AGjeStP4RkFZCkK6fru2EasqPNlW6xNMAY130_provenance.
- NP652033.RAVmTp_naw9AGjeStP4RkFZCkK6fru2EasqPNlW6xNMAY130_assertion evidence source_evidence_literature NP652033.RAVmTp_naw9AGjeStP4RkFZCkK6fru2EasqPNlW6xNMAY130_provenance.
- NP652033.RAVmTp_naw9AGjeStP4RkFZCkK6fru2EasqPNlW6xNMAY130_assertion SIO_000772 1822343 NP652033.RAVmTp_naw9AGjeStP4RkFZCkK6fru2EasqPNlW6xNMAY130_provenance.
- NP652033.RAVmTp_naw9AGjeStP4RkFZCkK6fru2EasqPNlW6xNMAY130_assertion wasDerivedFrom befree-2016 NP652033.RAVmTp_naw9AGjeStP4RkFZCkK6fru2EasqPNlW6xNMAY130_provenance.
- NP652033.RAVmTp_naw9AGjeStP4RkFZCkK6fru2EasqPNlW6xNMAY130_assertion wasGeneratedBy ECO_0000203 NP652033.RAVmTp_naw9AGjeStP4RkFZCkK6fru2EasqPNlW6xNMAY130_provenance.