Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP528881.RAAvUJK2NuwbArAsv-PRgeEOo4d7piY2h-8tSU3jsmT5U130_assertion> ?p ?o ?g. }
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- NP528881.RAAvUJK2NuwbArAsv-PRgeEOo4d7piY2h-8tSU3jsmT5U130_assertion type Assertion NP528881.RAAvUJK2NuwbArAsv-PRgeEOo4d7piY2h-8tSU3jsmT5U130_head.
- NP528881.RAAvUJK2NuwbArAsv-PRgeEOo4d7piY2h-8tSU3jsmT5U130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528881.RAAvUJK2NuwbArAsv-PRgeEOo4d7piY2h-8tSU3jsmT5U130_provenance.
- NP528881.RAAvUJK2NuwbArAsv-PRgeEOo4d7piY2h-8tSU3jsmT5U130_assertion evidence source_evidence_literature NP528881.RAAvUJK2NuwbArAsv-PRgeEOo4d7piY2h-8tSU3jsmT5U130_provenance.
- NP528881.RAAvUJK2NuwbArAsv-PRgeEOo4d7piY2h-8tSU3jsmT5U130_assertion SIO_000772 16384941 NP528881.RAAvUJK2NuwbArAsv-PRgeEOo4d7piY2h-8tSU3jsmT5U130_provenance.
- NP528881.RAAvUJK2NuwbArAsv-PRgeEOo4d7piY2h-8tSU3jsmT5U130_assertion wasDerivedFrom befree-2016 NP528881.RAAvUJK2NuwbArAsv-PRgeEOo4d7piY2h-8tSU3jsmT5U130_provenance.
- NP528881.RAAvUJK2NuwbArAsv-PRgeEOo4d7piY2h-8tSU3jsmT5U130_assertion wasGeneratedBy ECO_0000203 NP528881.RAAvUJK2NuwbArAsv-PRgeEOo4d7piY2h-8tSU3jsmT5U130_provenance.