Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP616127.RAMHbAN6OAj3DkW7sCbNaz6UfOPkQn5pi324M3X_54Zjg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP616127.RAMHbAN6OAj3DkW7sCbNaz6UfOPkQn5pi324M3X_54Zjg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616127.RAMHbAN6OAj3DkW7sCbNaz6UfOPkQn5pi324M3X_54Zjg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616127.RAMHbAN6OAj3DkW7sCbNaz6UfOPkQn5pi324M3X_54Zjg130_provenance.
- NP616127.RAMHbAN6OAj3DkW7sCbNaz6UfOPkQn5pi324M3X_54Zjg130_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." NP616127.RAMHbAN6OAj3DkW7sCbNaz6UfOPkQn5pi324M3X_54Zjg130_provenance.
- NP616127.RAMHbAN6OAj3DkW7sCbNaz6UfOPkQn5pi324M3X_54Zjg130_assertion evidence source_evidence_literature NP616127.RAMHbAN6OAj3DkW7sCbNaz6UfOPkQn5pi324M3X_54Zjg130_provenance.
- NP616127.RAMHbAN6OAj3DkW7sCbNaz6UfOPkQn5pi324M3X_54Zjg130_assertion SIO_000772 7643352 NP616127.RAMHbAN6OAj3DkW7sCbNaz6UfOPkQn5pi324M3X_54Zjg130_provenance.
- NP616127.RAMHbAN6OAj3DkW7sCbNaz6UfOPkQn5pi324M3X_54Zjg130_assertion wasDerivedFrom befree-20140225 NP616127.RAMHbAN6OAj3DkW7sCbNaz6UfOPkQn5pi324M3X_54Zjg130_provenance.
- NP616127.RAMHbAN6OAj3DkW7sCbNaz6UfOPkQn5pi324M3X_54Zjg130_assertion wasGeneratedBy ECO_0000203 NP616127.RAMHbAN6OAj3DkW7sCbNaz6UfOPkQn5pi324M3X_54Zjg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP616127.RAMHbAN6OAj3DkW7sCbNaz6UfOPkQn5pi324M3X_54Zjg130_provenance.