Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP28720.RA6HNagPpf4XGL2I4GxEP758KgbyHWx67DUQx6SOzFbfM130_assertion> ?p ?o ?g. }
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- NP28720.RA6HNagPpf4XGL2I4GxEP758KgbyHWx67DUQx6SOzFbfM130_assertion type Assertion NP28720.RA6HNagPpf4XGL2I4GxEP758KgbyHWx67DUQx6SOzFbfM130_head.
- NP28720.RA6HNagPpf4XGL2I4GxEP758KgbyHWx67DUQx6SOzFbfM130_assertion description "[Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP28720.RA6HNagPpf4XGL2I4GxEP758KgbyHWx67DUQx6SOzFbfM130_provenance.
- NP28720.RA6HNagPpf4XGL2I4GxEP758KgbyHWx67DUQx6SOzFbfM130_assertion evidence source_evidence_curated NP28720.RA6HNagPpf4XGL2I4GxEP758KgbyHWx67DUQx6SOzFbfM130_provenance.
- NP28720.RA6HNagPpf4XGL2I4GxEP758KgbyHWx67DUQx6SOzFbfM130_assertion SIO_000772 9326941 NP28720.RA6HNagPpf4XGL2I4GxEP758KgbyHWx67DUQx6SOzFbfM130_provenance.
- NP28720.RA6HNagPpf4XGL2I4GxEP758KgbyHWx67DUQx6SOzFbfM130_assertion wasDerivedFrom ctd_human-20150221 NP28720.RA6HNagPpf4XGL2I4GxEP758KgbyHWx67DUQx6SOzFbfM130_provenance.
- NP28720.RA6HNagPpf4XGL2I4GxEP758KgbyHWx67DUQx6SOzFbfM130_assertion wasGeneratedBy ECO_0000218 NP28720.RA6HNagPpf4XGL2I4GxEP758KgbyHWx67DUQx6SOzFbfM130_provenance.