Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP564824.RALXLkLtcwTZ82gM-rayV0p6pSRloV-szT_Eb4Kw4Is3o130_assertion> ?p ?o ?g. }
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- NP564824.RALXLkLtcwTZ82gM-rayV0p6pSRloV-szT_Eb4Kw4Is3o130_assertion type Assertion NP564824.RALXLkLtcwTZ82gM-rayV0p6pSRloV-szT_Eb4Kw4Is3o130_head.
- NP564824.RALXLkLtcwTZ82gM-rayV0p6pSRloV-szT_Eb4Kw4Is3o130_assertion description "[To identify suspected RDS mutations in families in which different people have been identified with either generalised retinal dystrophy or macular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP564824.RALXLkLtcwTZ82gM-rayV0p6pSRloV-szT_Eb4Kw4Is3o130_provenance.
- NP564824.RALXLkLtcwTZ82gM-rayV0p6pSRloV-szT_Eb4Kw4Is3o130_assertion evidence source_evidence_literature NP564824.RALXLkLtcwTZ82gM-rayV0p6pSRloV-szT_Eb4Kw4Is3o130_provenance.
- NP564824.RALXLkLtcwTZ82gM-rayV0p6pSRloV-szT_Eb4Kw4Is3o130_assertion SIO_000772 16916875 NP564824.RALXLkLtcwTZ82gM-rayV0p6pSRloV-szT_Eb4Kw4Is3o130_provenance.
- NP564824.RALXLkLtcwTZ82gM-rayV0p6pSRloV-szT_Eb4Kw4Is3o130_assertion wasDerivedFrom befree-2016 NP564824.RALXLkLtcwTZ82gM-rayV0p6pSRloV-szT_Eb4Kw4Is3o130_provenance.
- NP564824.RALXLkLtcwTZ82gM-rayV0p6pSRloV-szT_Eb4Kw4Is3o130_assertion wasGeneratedBy ECO_0000203 NP564824.RALXLkLtcwTZ82gM-rayV0p6pSRloV-szT_Eb4Kw4Is3o130_provenance.