Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418941.RAc95YS4yfTjnnEkT_4wVUn6bbN3i2eqAqJOjRapW0A_c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418941.RAc95YS4yfTjnnEkT_4wVUn6bbN3i2eqAqJOjRapW0A_c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418941.RAc95YS4yfTjnnEkT_4wVUn6bbN3i2eqAqJOjRapW0A_c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418941.RAc95YS4yfTjnnEkT_4wVUn6bbN3i2eqAqJOjRapW0A_c130_provenance.
- NP418941.RAc95YS4yfTjnnEkT_4wVUn6bbN3i2eqAqJOjRapW0A_c130_assertion description "[Mutations in keratin 1 and 10 have been identified in these patients and are similar to those mutations in patients with classic epidermolytic hyperkeratosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418941.RAc95YS4yfTjnnEkT_4wVUn6bbN3i2eqAqJOjRapW0A_c130_provenance.
- NP418941.RAc95YS4yfTjnnEkT_4wVUn6bbN3i2eqAqJOjRapW0A_c130_assertion evidence source_evidence_literature NP418941.RAc95YS4yfTjnnEkT_4wVUn6bbN3i2eqAqJOjRapW0A_c130_provenance.
- NP418941.RAc95YS4yfTjnnEkT_4wVUn6bbN3i2eqAqJOjRapW0A_c130_assertion SIO_000772 14594577 NP418941.RAc95YS4yfTjnnEkT_4wVUn6bbN3i2eqAqJOjRapW0A_c130_provenance.
- NP418941.RAc95YS4yfTjnnEkT_4wVUn6bbN3i2eqAqJOjRapW0A_c130_assertion wasDerivedFrom befree-2016 NP418941.RAc95YS4yfTjnnEkT_4wVUn6bbN3i2eqAqJOjRapW0A_c130_provenance.
- NP418941.RAc95YS4yfTjnnEkT_4wVUn6bbN3i2eqAqJOjRapW0A_c130_assertion wasGeneratedBy ECO_0000203 NP418941.RAc95YS4yfTjnnEkT_4wVUn6bbN3i2eqAqJOjRapW0A_c130_provenance.
- befree-2016 importedOn "2016-02-19" NP418941.RAc95YS4yfTjnnEkT_4wVUn6bbN3i2eqAqJOjRapW0A_c130_provenance.