Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1330983.RAy7mRB4Wx_ZKjPwYVD9Y0Gep1tbOyTVxk_tA8jUTEzZk130_assertion> ?p ?o ?g. }
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- NP1330983.RAy7mRB4Wx_ZKjPwYVD9Y0Gep1tbOyTVxk_tA8jUTEzZk130_assertion type Assertion NP1330983.RAy7mRB4Wx_ZKjPwYVD9Y0Gep1tbOyTVxk_tA8jUTEzZk130_head.
- NP1330983.RAy7mRB4Wx_ZKjPwYVD9Y0Gep1tbOyTVxk_tA8jUTEzZk130_assertion wasGeneratedBy ECO_0000203 NP1330983.RAy7mRB4Wx_ZKjPwYVD9Y0Gep1tbOyTVxk_tA8jUTEzZk130_provenance.
- NP1330983.RAy7mRB4Wx_ZKjPwYVD9Y0Gep1tbOyTVxk_tA8jUTEzZk130_assertion wasDerivedFrom befree-2016 NP1330983.RAy7mRB4Wx_ZKjPwYVD9Y0Gep1tbOyTVxk_tA8jUTEzZk130_provenance.
- NP1330983.RAy7mRB4Wx_ZKjPwYVD9Y0Gep1tbOyTVxk_tA8jUTEzZk130_assertion SIO_000772 8058286 NP1330983.RAy7mRB4Wx_ZKjPwYVD9Y0Gep1tbOyTVxk_tA8jUTEzZk130_provenance.
- NP1330983.RAy7mRB4Wx_ZKjPwYVD9Y0Gep1tbOyTVxk_tA8jUTEzZk130_assertion evidence source_evidence_literature NP1330983.RAy7mRB4Wx_ZKjPwYVD9Y0Gep1tbOyTVxk_tA8jUTEzZk130_provenance.
- NP1330983.RAy7mRB4Wx_ZKjPwYVD9Y0Gep1tbOyTVxk_tA8jUTEzZk130_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." NP1330983.RAy7mRB4Wx_ZKjPwYVD9Y0Gep1tbOyTVxk_tA8jUTEzZk130_provenance.