Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_assertion type Assertion NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_head.
- NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_assertion wasGeneratedBy ECO_0000203 NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_provenance.
- NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_assertion wasDerivedFrom befree-2016 NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_provenance.
- NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_assertion SIO_000772 8058286 NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_provenance.
- NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_assertion evidence source_evidence_literature NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_provenance.
- NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_assertion description "[Clinical features of a previously undescribed codon 216 (proline to serine) mutation in the peripherin/retinal degeneration slow gene in autosomal dominant retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1330982.RALMJkZs-rNmhdhNHd1xUl47NaSNRzjJXPJPDY8zKmDZI130_provenance.