Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP869559.RAWj4rObwj2MSxGfYXYprVH_HSpdlOhMb4q2v30ywwr2Q130_assertion> ?p ?o ?g. }
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- NP869559.RAWj4rObwj2MSxGfYXYprVH_HSpdlOhMb4q2v30ywwr2Q130_assertion type Assertion NP869559.RAWj4rObwj2MSxGfYXYprVH_HSpdlOhMb4q2v30ywwr2Q130_head.
- NP869559.RAWj4rObwj2MSxGfYXYprVH_HSpdlOhMb4q2v30ywwr2Q130_assertion wasGeneratedBy ECO_0000203 NP869559.RAWj4rObwj2MSxGfYXYprVH_HSpdlOhMb4q2v30ywwr2Q130_provenance.
- NP869559.RAWj4rObwj2MSxGfYXYprVH_HSpdlOhMb4q2v30ywwr2Q130_assertion wasDerivedFrom befree-20140225 NP869559.RAWj4rObwj2MSxGfYXYprVH_HSpdlOhMb4q2v30ywwr2Q130_provenance.
- NP869559.RAWj4rObwj2MSxGfYXYprVH_HSpdlOhMb4q2v30ywwr2Q130_assertion SIO_000772 12679481 NP869559.RAWj4rObwj2MSxGfYXYprVH_HSpdlOhMb4q2v30ywwr2Q130_provenance.
- NP869559.RAWj4rObwj2MSxGfYXYprVH_HSpdlOhMb4q2v30ywwr2Q130_assertion evidence source_evidence_literature NP869559.RAWj4rObwj2MSxGfYXYprVH_HSpdlOhMb4q2v30ywwr2Q130_provenance.
- NP869559.RAWj4rObwj2MSxGfYXYprVH_HSpdlOhMb4q2v30ywwr2Q130_assertion description "[We conclude that a diverse spectrum of mutations in the HSD3B7 gene underlies this rare form of neonatal cholestasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869559.RAWj4rObwj2MSxGfYXYprVH_HSpdlOhMb4q2v30ywwr2Q130_provenance.