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- source_evidence_literature type ECO_0000212 NP872872.RAZ3NciwTl9NbpguVPifLkrLIzUhrZR9xQcMaxCEA4Kxs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP872872.RAZ3NciwTl9NbpguVPifLkrLIzUhrZR9xQcMaxCEA4Kxs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP872872.RAZ3NciwTl9NbpguVPifLkrLIzUhrZR9xQcMaxCEA4Kxs130_provenance.
- NP872872.RAZ3NciwTl9NbpguVPifLkrLIzUhrZR9xQcMaxCEA4Kxs130_assertion description "[This study adds sIBM and hereditary inclusion body myopathies to the growing list of TDP-43 positive inclusion diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872872.RAZ3NciwTl9NbpguVPifLkrLIzUhrZR9xQcMaxCEA4Kxs130_provenance.
- NP872872.RAZ3NciwTl9NbpguVPifLkrLIzUhrZR9xQcMaxCEA4Kxs130_assertion evidence source_evidence_literature NP872872.RAZ3NciwTl9NbpguVPifLkrLIzUhrZR9xQcMaxCEA4Kxs130_provenance.
- NP872872.RAZ3NciwTl9NbpguVPifLkrLIzUhrZR9xQcMaxCEA4Kxs130_assertion SIO_000772 18796596 NP872872.RAZ3NciwTl9NbpguVPifLkrLIzUhrZR9xQcMaxCEA4Kxs130_provenance.
- NP872872.RAZ3NciwTl9NbpguVPifLkrLIzUhrZR9xQcMaxCEA4Kxs130_assertion wasDerivedFrom befree-20150227 NP872872.RAZ3NciwTl9NbpguVPifLkrLIzUhrZR9xQcMaxCEA4Kxs130_provenance.
- NP872872.RAZ3NciwTl9NbpguVPifLkrLIzUhrZR9xQcMaxCEA4Kxs130_assertion wasGeneratedBy ECO_0000203 NP872872.RAZ3NciwTl9NbpguVPifLkrLIzUhrZR9xQcMaxCEA4Kxs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP872872.RAZ3NciwTl9NbpguVPifLkrLIzUhrZR9xQcMaxCEA4Kxs130_provenance.