Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_provenance.
- NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_assertion description "[This family represents a new syndrome (Mohr-Tranebjaerg syndrome, MTS) and provides significant new information about a new X linked recessive sydromic type of deafness which was previously thought to be isolated deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_provenance.
- NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_assertion evidence source_evidence_literature NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_provenance.
- NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_assertion SIO_000772 7643352 NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_provenance.
- NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_assertion wasDerivedFrom befree-20150227 NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_provenance.
- NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_assertion wasGeneratedBy ECO_0000203 NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP792669.RA7_X0a95kAAMVEALdjK9SBhelQ1RJBQcIPaGtG1jNvSA130_provenance.