Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP370668.RAtQy3yhscPqbYmBxm6mmd4c8c5ED0atJQw3O1O1VHiBo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP370668.RAtQy3yhscPqbYmBxm6mmd4c8c5ED0atJQw3O1O1VHiBo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP370668.RAtQy3yhscPqbYmBxm6mmd4c8c5ED0atJQw3O1O1VHiBo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP370668.RAtQy3yhscPqbYmBxm6mmd4c8c5ED0atJQw3O1O1VHiBo130_provenance.
- NP370668.RAtQy3yhscPqbYmBxm6mmd4c8c5ED0atJQw3O1O1VHiBo130_assertion wasGeneratedBy ECO_0000203 NP370668.RAtQy3yhscPqbYmBxm6mmd4c8c5ED0atJQw3O1O1VHiBo130_provenance.
- NP370668.RAtQy3yhscPqbYmBxm6mmd4c8c5ED0atJQw3O1O1VHiBo130_assertion wasDerivedFrom befree-20140225 NP370668.RAtQy3yhscPqbYmBxm6mmd4c8c5ED0atJQw3O1O1VHiBo130_provenance.
- NP370668.RAtQy3yhscPqbYmBxm6mmd4c8c5ED0atJQw3O1O1VHiBo130_assertion SIO_000772 14684684 NP370668.RAtQy3yhscPqbYmBxm6mmd4c8c5ED0atJQw3O1O1VHiBo130_provenance.
- NP370668.RAtQy3yhscPqbYmBxm6mmd4c8c5ED0atJQw3O1O1VHiBo130_assertion evidence source_evidence_literature NP370668.RAtQy3yhscPqbYmBxm6mmd4c8c5ED0atJQw3O1O1VHiBo130_provenance.
- NP370668.RAtQy3yhscPqbYmBxm6mmd4c8c5ED0atJQw3O1O1VHiBo130_assertion description "[A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP370668.RAtQy3yhscPqbYmBxm6mmd4c8c5ED0atJQw3O1O1VHiBo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP370668.RAtQy3yhscPqbYmBxm6mmd4c8c5ED0atJQw3O1O1VHiBo130_provenance.