Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP441140.RAF3p3bLqSgw0OnAVxBy8nLBBXxQSCd_x-XR8Rs_RsHcU130_assertion> ?p ?o ?g. }
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- NP441140.RAF3p3bLqSgw0OnAVxBy8nLBBXxQSCd_x-XR8Rs_RsHcU130_assertion type Assertion NP441140.RAF3p3bLqSgw0OnAVxBy8nLBBXxQSCd_x-XR8Rs_RsHcU130_head.
- NP441140.RAF3p3bLqSgw0OnAVxBy8nLBBXxQSCd_x-XR8Rs_RsHcU130_assertion description "[We have searched for mutations in the maleylacetoacetate isomerase gene in four cases of unexplained severe liver failure in infancy with clinical similarities to hereditary tyrosinemia type I (pseudotyrosinemia).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441140.RAF3p3bLqSgw0OnAVxBy8nLBBXxQSCd_x-XR8Rs_RsHcU130_provenance.
- NP441140.RAF3p3bLqSgw0OnAVxBy8nLBBXxQSCd_x-XR8Rs_RsHcU130_assertion evidence source_evidence_literature NP441140.RAF3p3bLqSgw0OnAVxBy8nLBBXxQSCd_x-XR8Rs_RsHcU130_provenance.
- NP441140.RAF3p3bLqSgw0OnAVxBy8nLBBXxQSCd_x-XR8Rs_RsHcU130_assertion SIO_000772 10373324 NP441140.RAF3p3bLqSgw0OnAVxBy8nLBBXxQSCd_x-XR8Rs_RsHcU130_provenance.
- NP441140.RAF3p3bLqSgw0OnAVxBy8nLBBXxQSCd_x-XR8Rs_RsHcU130_assertion wasDerivedFrom befree-20150227 NP441140.RAF3p3bLqSgw0OnAVxBy8nLBBXxQSCd_x-XR8Rs_RsHcU130_provenance.
- NP441140.RAF3p3bLqSgw0OnAVxBy8nLBBXxQSCd_x-XR8Rs_RsHcU130_assertion wasGeneratedBy ECO_0000203 NP441140.RAF3p3bLqSgw0OnAVxBy8nLBBXxQSCd_x-XR8Rs_RsHcU130_provenance.