Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP414283.RA13VP5sAOblE-dYxnVtg2f-hdnfb1FUAR3mJcJsjzwUs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP414283.RA13VP5sAOblE-dYxnVtg2f-hdnfb1FUAR3mJcJsjzwUs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP414283.RA13VP5sAOblE-dYxnVtg2f-hdnfb1FUAR3mJcJsjzwUs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP414283.RA13VP5sAOblE-dYxnVtg2f-hdnfb1FUAR3mJcJsjzwUs130_provenance.
- NP414283.RA13VP5sAOblE-dYxnVtg2f-hdnfb1FUAR3mJcJsjzwUs130_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." NP414283.RA13VP5sAOblE-dYxnVtg2f-hdnfb1FUAR3mJcJsjzwUs130_provenance.
- NP414283.RA13VP5sAOblE-dYxnVtg2f-hdnfb1FUAR3mJcJsjzwUs130_assertion evidence source_evidence_literature NP414283.RA13VP5sAOblE-dYxnVtg2f-hdnfb1FUAR3mJcJsjzwUs130_provenance.
- NP414283.RA13VP5sAOblE-dYxnVtg2f-hdnfb1FUAR3mJcJsjzwUs130_assertion SIO_000772 19349200 NP414283.RA13VP5sAOblE-dYxnVtg2f-hdnfb1FUAR3mJcJsjzwUs130_provenance.
- NP414283.RA13VP5sAOblE-dYxnVtg2f-hdnfb1FUAR3mJcJsjzwUs130_assertion wasDerivedFrom befree-20140225 NP414283.RA13VP5sAOblE-dYxnVtg2f-hdnfb1FUAR3mJcJsjzwUs130_provenance.
- NP414283.RA13VP5sAOblE-dYxnVtg2f-hdnfb1FUAR3mJcJsjzwUs130_assertion wasGeneratedBy ECO_0000203 NP414283.RA13VP5sAOblE-dYxnVtg2f-hdnfb1FUAR3mJcJsjzwUs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP414283.RA13VP5sAOblE-dYxnVtg2f-hdnfb1FUAR3mJcJsjzwUs130_provenance.