Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP730775.RAEW2sdr8b4wvBdxC-rDpTOwebbFNWw9Dh4aIy41V_TWU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP730775.RAEW2sdr8b4wvBdxC-rDpTOwebbFNWw9Dh4aIy41V_TWU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP730775.RAEW2sdr8b4wvBdxC-rDpTOwebbFNWw9Dh4aIy41V_TWU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP730775.RAEW2sdr8b4wvBdxC-rDpTOwebbFNWw9Dh4aIy41V_TWU130_provenance.
- NP730775.RAEW2sdr8b4wvBdxC-rDpTOwebbFNWw9Dh4aIy41V_TWU130_assertion description "[Two new mutations in the MT-TW gene leading to the disruption of the secondary structure of the tRNA(Trp) in patients with Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP730775.RAEW2sdr8b4wvBdxC-rDpTOwebbFNWw9Dh4aIy41V_TWU130_provenance.
- NP730775.RAEW2sdr8b4wvBdxC-rDpTOwebbFNWw9Dh4aIy41V_TWU130_assertion evidence source_evidence_literature NP730775.RAEW2sdr8b4wvBdxC-rDpTOwebbFNWw9Dh4aIy41V_TWU130_provenance.
- NP730775.RAEW2sdr8b4wvBdxC-rDpTOwebbFNWw9Dh4aIy41V_TWU130_assertion SIO_000772 19349200 NP730775.RAEW2sdr8b4wvBdxC-rDpTOwebbFNWw9Dh4aIy41V_TWU130_provenance.
- NP730775.RAEW2sdr8b4wvBdxC-rDpTOwebbFNWw9Dh4aIy41V_TWU130_assertion wasDerivedFrom befree-2016 NP730775.RAEW2sdr8b4wvBdxC-rDpTOwebbFNWw9Dh4aIy41V_TWU130_provenance.
- NP730775.RAEW2sdr8b4wvBdxC-rDpTOwebbFNWw9Dh4aIy41V_TWU130_assertion wasGeneratedBy ECO_0000203 NP730775.RAEW2sdr8b4wvBdxC-rDpTOwebbFNWw9Dh4aIy41V_TWU130_provenance.
- befree-2016 importedOn "2016-02-19" NP730775.RAEW2sdr8b4wvBdxC-rDpTOwebbFNWw9Dh4aIy41V_TWU130_provenance.