Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1238020.RA38TWbvlrWGLnm7ZIZL7hWlBtK9j0zLcDPVQ57hKiL_U130_assertion> ?p ?o ?g. }
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- NP1238020.RA38TWbvlrWGLnm7ZIZL7hWlBtK9j0zLcDPVQ57hKiL_U130_assertion type Assertion NP1238020.RA38TWbvlrWGLnm7ZIZL7hWlBtK9j0zLcDPVQ57hKiL_U130_head.
- NP1238020.RA38TWbvlrWGLnm7ZIZL7hWlBtK9j0zLcDPVQ57hKiL_U130_assertion description "[Exome sequencing identifies novel and recurrent mutations in GJA8 and CRYGD associated with inherited cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1238020.RA38TWbvlrWGLnm7ZIZL7hWlBtK9j0zLcDPVQ57hKiL_U130_provenance.
- NP1238020.RA38TWbvlrWGLnm7ZIZL7hWlBtK9j0zLcDPVQ57hKiL_U130_assertion evidence source_evidence_literature NP1238020.RA38TWbvlrWGLnm7ZIZL7hWlBtK9j0zLcDPVQ57hKiL_U130_provenance.
- NP1238020.RA38TWbvlrWGLnm7ZIZL7hWlBtK9j0zLcDPVQ57hKiL_U130_assertion SIO_000772 25403472 NP1238020.RA38TWbvlrWGLnm7ZIZL7hWlBtK9j0zLcDPVQ57hKiL_U130_provenance.
- NP1238020.RA38TWbvlrWGLnm7ZIZL7hWlBtK9j0zLcDPVQ57hKiL_U130_assertion wasDerivedFrom befree-2016 NP1238020.RA38TWbvlrWGLnm7ZIZL7hWlBtK9j0zLcDPVQ57hKiL_U130_provenance.
- NP1238020.RA38TWbvlrWGLnm7ZIZL7hWlBtK9j0zLcDPVQ57hKiL_U130_assertion wasGeneratedBy ECO_0000203 NP1238020.RA38TWbvlrWGLnm7ZIZL7hWlBtK9j0zLcDPVQ57hKiL_U130_provenance.