Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP844912.RAZrNMYqxCvPoo8yMp_qR27lrYXnMc9UiajKR08K0ckkQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP844912.RAZrNMYqxCvPoo8yMp_qR27lrYXnMc9UiajKR08K0ckkQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP844912.RAZrNMYqxCvPoo8yMp_qR27lrYXnMc9UiajKR08K0ckkQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP844912.RAZrNMYqxCvPoo8yMp_qR27lrYXnMc9UiajKR08K0ckkQ130_provenance.
- NP844912.RAZrNMYqxCvPoo8yMp_qR27lrYXnMc9UiajKR08K0ckkQ130_assertion description "[In addition to sat-1 and prestin, which were cloned from rat and gerbil, respectively, three human members have been identified and associated with specific genetic diseases (DTD, diastrophic dysplasia; CLD, congenital chloride diarrhea; PDS, Pendred syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844912.RAZrNMYqxCvPoo8yMp_qR27lrYXnMc9UiajKR08K0ckkQ130_provenance.
- NP844912.RAZrNMYqxCvPoo8yMp_qR27lrYXnMc9UiajKR08K0ckkQ130_assertion evidence source_evidence_literature NP844912.RAZrNMYqxCvPoo8yMp_qR27lrYXnMc9UiajKR08K0ckkQ130_provenance.
- NP844912.RAZrNMYqxCvPoo8yMp_qR27lrYXnMc9UiajKR08K0ckkQ130_assertion SIO_000772 11247665 NP844912.RAZrNMYqxCvPoo8yMp_qR27lrYXnMc9UiajKR08K0ckkQ130_provenance.
- NP844912.RAZrNMYqxCvPoo8yMp_qR27lrYXnMc9UiajKR08K0ckkQ130_assertion wasDerivedFrom befree-20140225 NP844912.RAZrNMYqxCvPoo8yMp_qR27lrYXnMc9UiajKR08K0ckkQ130_provenance.
- NP844912.RAZrNMYqxCvPoo8yMp_qR27lrYXnMc9UiajKR08K0ckkQ130_assertion wasGeneratedBy ECO_0000203 NP844912.RAZrNMYqxCvPoo8yMp_qR27lrYXnMc9UiajKR08K0ckkQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP844912.RAZrNMYqxCvPoo8yMp_qR27lrYXnMc9UiajKR08K0ckkQ130_provenance.