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- NP857473.RAD_T08JaHKTMRoFH08IlDDKvgwPm3iVFXsc6GOTlAOkY130_assertion type Assertion NP857473.RAD_T08JaHKTMRoFH08IlDDKvgwPm3iVFXsc6GOTlAOkY130_head.
- NP857473.RAD_T08JaHKTMRoFH08IlDDKvgwPm3iVFXsc6GOTlAOkY130_assertion description "[Mutations in the retinitis pigmentosa 1 (RP1) gene are a common cause of autosomal dominant retinitis pigmentosa (adRP), and have also been found to cause autosomal recessive RP (arRP) in a few families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857473.RAD_T08JaHKTMRoFH08IlDDKvgwPm3iVFXsc6GOTlAOkY130_provenance.
- NP857473.RAD_T08JaHKTMRoFH08IlDDKvgwPm3iVFXsc6GOTlAOkY130_assertion evidence source_evidence_literature NP857473.RAD_T08JaHKTMRoFH08IlDDKvgwPm3iVFXsc6GOTlAOkY130_provenance.
- NP857473.RAD_T08JaHKTMRoFH08IlDDKvgwPm3iVFXsc6GOTlAOkY130_assertion SIO_000772 22927954 NP857473.RAD_T08JaHKTMRoFH08IlDDKvgwPm3iVFXsc6GOTlAOkY130_provenance.
- NP857473.RAD_T08JaHKTMRoFH08IlDDKvgwPm3iVFXsc6GOTlAOkY130_assertion wasDerivedFrom befree-20150227 NP857473.RAD_T08JaHKTMRoFH08IlDDKvgwPm3iVFXsc6GOTlAOkY130_provenance.
- NP857473.RAD_T08JaHKTMRoFH08IlDDKvgwPm3iVFXsc6GOTlAOkY130_assertion wasGeneratedBy ECO_0000203 NP857473.RAD_T08JaHKTMRoFH08IlDDKvgwPm3iVFXsc6GOTlAOkY130_provenance.