Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP766306.RApqMiTaWLyz-6wS7d4kEqkr-gERBK-eRmihiRgbX2pzM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP766306.RApqMiTaWLyz-6wS7d4kEqkr-gERBK-eRmihiRgbX2pzM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP766306.RApqMiTaWLyz-6wS7d4kEqkr-gERBK-eRmihiRgbX2pzM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP766306.RApqMiTaWLyz-6wS7d4kEqkr-gERBK-eRmihiRgbX2pzM130_provenance.
- NP766306.RApqMiTaWLyz-6wS7d4kEqkr-gERBK-eRmihiRgbX2pzM130_assertion description "[The PDS gene (7q31), responsible for Pendred syndrome (congenital sensorineural hearing loss and goiter), encodes a transmembrane protein known as pendrin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766306.RApqMiTaWLyz-6wS7d4kEqkr-gERBK-eRmihiRgbX2pzM130_provenance.
- NP766306.RApqMiTaWLyz-6wS7d4kEqkr-gERBK-eRmihiRgbX2pzM130_assertion evidence source_evidence_literature NP766306.RApqMiTaWLyz-6wS7d4kEqkr-gERBK-eRmihiRgbX2pzM130_provenance.
- NP766306.RApqMiTaWLyz-6wS7d4kEqkr-gERBK-eRmihiRgbX2pzM130_assertion SIO_000772 12727986 NP766306.RApqMiTaWLyz-6wS7d4kEqkr-gERBK-eRmihiRgbX2pzM130_provenance.
- NP766306.RApqMiTaWLyz-6wS7d4kEqkr-gERBK-eRmihiRgbX2pzM130_assertion wasDerivedFrom befree-20140225 NP766306.RApqMiTaWLyz-6wS7d4kEqkr-gERBK-eRmihiRgbX2pzM130_provenance.
- NP766306.RApqMiTaWLyz-6wS7d4kEqkr-gERBK-eRmihiRgbX2pzM130_assertion wasGeneratedBy ECO_0000203 NP766306.RApqMiTaWLyz-6wS7d4kEqkr-gERBK-eRmihiRgbX2pzM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP766306.RApqMiTaWLyz-6wS7d4kEqkr-gERBK-eRmihiRgbX2pzM130_provenance.