Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP277020.RAX38OqdBBh4DiC-Hzu9E2g1EljVr5kE5wKf3CwiR_noc130_assertion> ?p ?o ?g. }
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- NP277020.RAX38OqdBBh4DiC-Hzu9E2g1EljVr5kE5wKf3CwiR_noc130_assertion type Assertion NP277020.RAX38OqdBBh4DiC-Hzu9E2g1EljVr5kE5wKf3CwiR_noc130_head.
- NP277020.RAX38OqdBBh4DiC-Hzu9E2g1EljVr5kE5wKf3CwiR_noc130_assertion description "[The retinal degeneration in this patient is most likely to be secondary to a genetic disorder of autosomal or X-linked recessive inheritance rather than SCA6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277020.RAX38OqdBBh4DiC-Hzu9E2g1EljVr5kE5wKf3CwiR_noc130_provenance.
- NP277020.RAX38OqdBBh4DiC-Hzu9E2g1EljVr5kE5wKf3CwiR_noc130_assertion evidence source_evidence_literature NP277020.RAX38OqdBBh4DiC-Hzu9E2g1EljVr5kE5wKf3CwiR_noc130_provenance.
- NP277020.RAX38OqdBBh4DiC-Hzu9E2g1EljVr5kE5wKf3CwiR_noc130_assertion SIO_000772 12081723 NP277020.RAX38OqdBBh4DiC-Hzu9E2g1EljVr5kE5wKf3CwiR_noc130_provenance.
- NP277020.RAX38OqdBBh4DiC-Hzu9E2g1EljVr5kE5wKf3CwiR_noc130_assertion wasDerivedFrom befree-20150227 NP277020.RAX38OqdBBh4DiC-Hzu9E2g1EljVr5kE5wKf3CwiR_noc130_provenance.
- NP277020.RAX38OqdBBh4DiC-Hzu9E2g1EljVr5kE5wKf3CwiR_noc130_assertion wasGeneratedBy ECO_0000203 NP277020.RAX38OqdBBh4DiC-Hzu9E2g1EljVr5kE5wKf3CwiR_noc130_provenance.