Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP616127.RAMHbAN6OAj3DkW7sCbNaz6UfOPkQn5pi324M3X_54Zjg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP616127.RAMHbAN6OAj3DkW7sCbNaz6UfOPkQn5pi324M3X_54Zjg130_assertion type Assertion NP616127.RAMHbAN6OAj3DkW7sCbNaz6UfOPkQn5pi324M3X_54Zjg130_head.
- 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.