Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP716219.RAydmJJBvbkMjx4xja7dCCK5yviQEpO5e-K_MvGHzksyo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP716219.RAydmJJBvbkMjx4xja7dCCK5yviQEpO5e-K_MvGHzksyo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP716219.RAydmJJBvbkMjx4xja7dCCK5yviQEpO5e-K_MvGHzksyo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP716219.RAydmJJBvbkMjx4xja7dCCK5yviQEpO5e-K_MvGHzksyo130_provenance.
- NP716219.RAydmJJBvbkMjx4xja7dCCK5yviQEpO5e-K_MvGHzksyo130_assertion description "[Recurrent R162W mutation ofkeratin 9 has been reported in multiple families with epidermolytic hyperkeratosis (EHK)-type hereditary palmoplantar keratoderma (PPK).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP716219.RAydmJJBvbkMjx4xja7dCCK5yviQEpO5e-K_MvGHzksyo130_provenance.
- NP716219.RAydmJJBvbkMjx4xja7dCCK5yviQEpO5e-K_MvGHzksyo130_assertion evidence source_evidence_literature NP716219.RAydmJJBvbkMjx4xja7dCCK5yviQEpO5e-K_MvGHzksyo130_provenance.
- NP716219.RAydmJJBvbkMjx4xja7dCCK5yviQEpO5e-K_MvGHzksyo130_assertion SIO_000772 10536990 NP716219.RAydmJJBvbkMjx4xja7dCCK5yviQEpO5e-K_MvGHzksyo130_provenance.
- NP716219.RAydmJJBvbkMjx4xja7dCCK5yviQEpO5e-K_MvGHzksyo130_assertion wasDerivedFrom befree-20140225 NP716219.RAydmJJBvbkMjx4xja7dCCK5yviQEpO5e-K_MvGHzksyo130_provenance.
- NP716219.RAydmJJBvbkMjx4xja7dCCK5yviQEpO5e-K_MvGHzksyo130_assertion wasGeneratedBy ECO_0000203 NP716219.RAydmJJBvbkMjx4xja7dCCK5yviQEpO5e-K_MvGHzksyo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP716219.RAydmJJBvbkMjx4xja7dCCK5yviQEpO5e-K_MvGHzksyo130_provenance.