Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP546603.RABN9V4RCL3pEap-dc3kn0l9bn2zynv_9pdSjMgyVcgLs130_assertion> ?p ?o ?g. }
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- NP546603.RABN9V4RCL3pEap-dc3kn0l9bn2zynv_9pdSjMgyVcgLs130_assertion type Assertion NP546603.RABN9V4RCL3pEap-dc3kn0l9bn2zynv_9pdSjMgyVcgLs130_head.
- NP546603.RABN9V4RCL3pEap-dc3kn0l9bn2zynv_9pdSjMgyVcgLs130_assertion wasGeneratedBy ECO_0000203 NP546603.RABN9V4RCL3pEap-dc3kn0l9bn2zynv_9pdSjMgyVcgLs130_provenance.
- NP546603.RABN9V4RCL3pEap-dc3kn0l9bn2zynv_9pdSjMgyVcgLs130_assertion wasDerivedFrom befree-2016 NP546603.RABN9V4RCL3pEap-dc3kn0l9bn2zynv_9pdSjMgyVcgLs130_provenance.
- NP546603.RABN9V4RCL3pEap-dc3kn0l9bn2zynv_9pdSjMgyVcgLs130_assertion SIO_000772 16636649 NP546603.RABN9V4RCL3pEap-dc3kn0l9bn2zynv_9pdSjMgyVcgLs130_provenance.
- NP546603.RABN9V4RCL3pEap-dc3kn0l9bn2zynv_9pdSjMgyVcgLs130_assertion evidence source_evidence_literature NP546603.RABN9V4RCL3pEap-dc3kn0l9bn2zynv_9pdSjMgyVcgLs130_provenance.
- NP546603.RABN9V4RCL3pEap-dc3kn0l9bn2zynv_9pdSjMgyVcgLs130_assertion description "[Expanding the mutational spectrum in TGFBI-linked corneal dystrophies: Identification of a novel and unusual mutation (Val113Ile) in a family with granular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP546603.RABN9V4RCL3pEap-dc3kn0l9bn2zynv_9pdSjMgyVcgLs130_provenance.