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- source_evidence_literature type ECO_0000212 NP294883.RA81-u-fp_v6uArQaPjWzzLKMxOZfXocee7hEkQZf0dvA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294883.RA81-u-fp_v6uArQaPjWzzLKMxOZfXocee7hEkQZf0dvA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294883.RA81-u-fp_v6uArQaPjWzzLKMxOZfXocee7hEkQZf0dvA130_provenance.
- NP294883.RA81-u-fp_v6uArQaPjWzzLKMxOZfXocee7hEkQZf0dvA130_assertion description "[These results suggest that the different types of Cx26 mutations affect autosomal recessive NSHL according to ethnic background.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294883.RA81-u-fp_v6uArQaPjWzzLKMxOZfXocee7hEkQZf0dvA130_provenance.
- NP294883.RA81-u-fp_v6uArQaPjWzzLKMxOZfXocee7hEkQZf0dvA130_assertion evidence source_evidence_literature NP294883.RA81-u-fp_v6uArQaPjWzzLKMxOZfXocee7hEkQZf0dvA130_provenance.
- NP294883.RA81-u-fp_v6uArQaPjWzzLKMxOZfXocee7hEkQZf0dvA130_assertion SIO_000772 10983956 NP294883.RA81-u-fp_v6uArQaPjWzzLKMxOZfXocee7hEkQZf0dvA130_provenance.
- NP294883.RA81-u-fp_v6uArQaPjWzzLKMxOZfXocee7hEkQZf0dvA130_assertion wasDerivedFrom befree-2016 NP294883.RA81-u-fp_v6uArQaPjWzzLKMxOZfXocee7hEkQZf0dvA130_provenance.
- NP294883.RA81-u-fp_v6uArQaPjWzzLKMxOZfXocee7hEkQZf0dvA130_assertion wasGeneratedBy ECO_0000203 NP294883.RA81-u-fp_v6uArQaPjWzzLKMxOZfXocee7hEkQZf0dvA130_provenance.
- befree-2016 importedOn "2016-02-19" NP294883.RA81-u-fp_v6uArQaPjWzzLKMxOZfXocee7hEkQZf0dvA130_provenance.