Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP723031.RAC1FqKp-QSriIv4L3Gpv5yC9RmRQSdPTti1QKBziALek130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP723031.RAC1FqKp-QSriIv4L3Gpv5yC9RmRQSdPTti1QKBziALek130_assertion type Assertion NP723031.RAC1FqKp-QSriIv4L3Gpv5yC9RmRQSdPTti1QKBziALek130_head.
- NP723031.RAC1FqKp-QSriIv4L3Gpv5yC9RmRQSdPTti1QKBziALek130_assertion description "[In addition, ABCR mutations were identified in families with recessive retinitis pigmentosa (RP), cone dystrophy (COD), and cone-rod dystrophy (CRD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723031.RAC1FqKp-QSriIv4L3Gpv5yC9RmRQSdPTti1QKBziALek130_provenance.
- NP723031.RAC1FqKp-QSriIv4L3Gpv5yC9RmRQSdPTti1QKBziALek130_assertion evidence source_evidence_literature NP723031.RAC1FqKp-QSriIv4L3Gpv5yC9RmRQSdPTti1QKBziALek130_provenance.
- NP723031.RAC1FqKp-QSriIv4L3Gpv5yC9RmRQSdPTti1QKBziALek130_assertion SIO_000772 9810566 NP723031.RAC1FqKp-QSriIv4L3Gpv5yC9RmRQSdPTti1QKBziALek130_provenance.
- NP723031.RAC1FqKp-QSriIv4L3Gpv5yC9RmRQSdPTti1QKBziALek130_assertion wasDerivedFrom befree-20140225 NP723031.RAC1FqKp-QSriIv4L3Gpv5yC9RmRQSdPTti1QKBziALek130_provenance.
- NP723031.RAC1FqKp-QSriIv4L3Gpv5yC9RmRQSdPTti1QKBziALek130_assertion wasGeneratedBy ECO_0000203 NP723031.RAC1FqKp-QSriIv4L3Gpv5yC9RmRQSdPTti1QKBziALek130_provenance.