Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_assertion> ?p ?o ?g. }
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- NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_assertion type Assertion NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_head.
- NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_assertion wasGeneratedBy ECO_0000203 NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_provenance.
- NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_assertion wasDerivedFrom befree-20150227 NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_provenance.
- NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_assertion SIO_000772 24405844 NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_provenance.
- NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_assertion evidence source_evidence_literature NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_provenance.
- NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_assertion description "[A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_provenance.