Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP591268.RAE4zAirn_nrR56FfnWND5AASC_bAe2_RTX-FhbLnL1lk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP591268.RAE4zAirn_nrR56FfnWND5AASC_bAe2_RTX-FhbLnL1lk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP591268.RAE4zAirn_nrR56FfnWND5AASC_bAe2_RTX-FhbLnL1lk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP591268.RAE4zAirn_nrR56FfnWND5AASC_bAe2_RTX-FhbLnL1lk130_provenance.
- NP591268.RAE4zAirn_nrR56FfnWND5AASC_bAe2_RTX-FhbLnL1lk130_assertion description "[The Hap 2/Hap 2 diplotype in MDR3 could therefore be potentially applied to DNA-based diagnosis in Japanese patients with PBC as a strong genetic biomarker for predicting the progression and prognosis of PBC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP591268.RAE4zAirn_nrR56FfnWND5AASC_bAe2_RTX-FhbLnL1lk130_provenance.
- NP591268.RAE4zAirn_nrR56FfnWND5AASC_bAe2_RTX-FhbLnL1lk130_assertion evidence source_evidence_literature NP591268.RAE4zAirn_nrR56FfnWND5AASC_bAe2_RTX-FhbLnL1lk130_provenance.
- NP591268.RAE4zAirn_nrR56FfnWND5AASC_bAe2_RTX-FhbLnL1lk130_assertion SIO_000772 18671305 NP591268.RAE4zAirn_nrR56FfnWND5AASC_bAe2_RTX-FhbLnL1lk130_provenance.
- NP591268.RAE4zAirn_nrR56FfnWND5AASC_bAe2_RTX-FhbLnL1lk130_assertion wasDerivedFrom befree-20150227 NP591268.RAE4zAirn_nrR56FfnWND5AASC_bAe2_RTX-FhbLnL1lk130_provenance.
- NP591268.RAE4zAirn_nrR56FfnWND5AASC_bAe2_RTX-FhbLnL1lk130_assertion wasGeneratedBy ECO_0000203 NP591268.RAE4zAirn_nrR56FfnWND5AASC_bAe2_RTX-FhbLnL1lk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP591268.RAE4zAirn_nrR56FfnWND5AASC_bAe2_RTX-FhbLnL1lk130_provenance.