Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1009066.RAyMLdYI5U-vJ28CrBImCdi8m82n4i1uwjXygCHy_3QRU130_provenance.
- 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.