Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP3999.RAt7SVJiUapFCbdgyTIGLyNGYYsnW5Lp2i4nb1i4bsLHo130_assertion> ?p ?o ?g. }
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- NP3999.RAt7SVJiUapFCbdgyTIGLyNGYYsnW5Lp2i4nb1i4bsLHo130_assertion type Assertion NP3999.RAt7SVJiUapFCbdgyTIGLyNGYYsnW5Lp2i4nb1i4bsLHo130_head.
- NP3999.RAt7SVJiUapFCbdgyTIGLyNGYYsnW5Lp2i4nb1i4bsLHo130_assertion description "[Allelic heterogeneity in the COH1 gene explains clinical variability in Cohen syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3999.RAt7SVJiUapFCbdgyTIGLyNGYYsnW5Lp2i4nb1i4bsLHo130_provenance.
- NP3999.RAt7SVJiUapFCbdgyTIGLyNGYYsnW5Lp2i4nb1i4bsLHo130_assertion evidence source_evidence_curated NP3999.RAt7SVJiUapFCbdgyTIGLyNGYYsnW5Lp2i4nb1i4bsLHo130_provenance.
- NP3999.RAt7SVJiUapFCbdgyTIGLyNGYYsnW5Lp2i4nb1i4bsLHo130_assertion SIO_000772 15154116 NP3999.RAt7SVJiUapFCbdgyTIGLyNGYYsnW5Lp2i4nb1i4bsLHo130_provenance.
- NP3999.RAt7SVJiUapFCbdgyTIGLyNGYYsnW5Lp2i4nb1i4bsLHo130_assertion wasDerivedFrom uniprot-20150221 NP3999.RAt7SVJiUapFCbdgyTIGLyNGYYsnW5Lp2i4nb1i4bsLHo130_provenance.
- NP3999.RAt7SVJiUapFCbdgyTIGLyNGYYsnW5Lp2i4nb1i4bsLHo130_assertion wasGeneratedBy ECO_0000218 NP3999.RAt7SVJiUapFCbdgyTIGLyNGYYsnW5Lp2i4nb1i4bsLHo130_provenance.