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- source_evidence_literature type ECO_0000212 NP576397.RADQIv922rYS6eeRZZPrp-rHYKn2_oWva8IQM9UeO6CN8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP576397.RADQIv922rYS6eeRZZPrp-rHYKn2_oWva8IQM9UeO6CN8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP576397.RADQIv922rYS6eeRZZPrp-rHYKn2_oWva8IQM9UeO6CN8130_provenance.
- NP576397.RADQIv922rYS6eeRZZPrp-rHYKn2_oWva8IQM9UeO6CN8130_assertion description "[Myotubularin (hMTM1), the founder member, is mutated in myotubular myopathy, and a close homolog (hMTMR2) was recently found mutated in a recessive form of Charcot-Marie-Tooth neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576397.RADQIv922rYS6eeRZZPrp-rHYKn2_oWva8IQM9UeO6CN8130_provenance.
- NP576397.RADQIv922rYS6eeRZZPrp-rHYKn2_oWva8IQM9UeO6CN8130_assertion evidence source_evidence_literature NP576397.RADQIv922rYS6eeRZZPrp-rHYKn2_oWva8IQM9UeO6CN8130_provenance.
- NP576397.RADQIv922rYS6eeRZZPrp-rHYKn2_oWva8IQM9UeO6CN8130_assertion SIO_000772 11275328 NP576397.RADQIv922rYS6eeRZZPrp-rHYKn2_oWva8IQM9UeO6CN8130_provenance.
- NP576397.RADQIv922rYS6eeRZZPrp-rHYKn2_oWva8IQM9UeO6CN8130_assertion wasDerivedFrom befree-20150227 NP576397.RADQIv922rYS6eeRZZPrp-rHYKn2_oWva8IQM9UeO6CN8130_provenance.
- NP576397.RADQIv922rYS6eeRZZPrp-rHYKn2_oWva8IQM9UeO6CN8130_assertion wasGeneratedBy ECO_0000203 NP576397.RADQIv922rYS6eeRZZPrp-rHYKn2_oWva8IQM9UeO6CN8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP576397.RADQIv922rYS6eeRZZPrp-rHYKn2_oWva8IQM9UeO6CN8130_provenance.