Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1018342.RAAjWIkMdD_tS64pMAZsmW9KJ3l2GKiNfwmdfqdG4H6MA130_assertion> ?p ?o ?g. }
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- NP1018342.RAAjWIkMdD_tS64pMAZsmW9KJ3l2GKiNfwmdfqdG4H6MA130_assertion type Assertion NP1018342.RAAjWIkMdD_tS64pMAZsmW9KJ3l2GKiNfwmdfqdG4H6MA130_head.
- NP1018342.RAAjWIkMdD_tS64pMAZsmW9KJ3l2GKiNfwmdfqdG4H6MA130_assertion wasGeneratedBy ECO_0000203 NP1018342.RAAjWIkMdD_tS64pMAZsmW9KJ3l2GKiNfwmdfqdG4H6MA130_provenance.
- NP1018342.RAAjWIkMdD_tS64pMAZsmW9KJ3l2GKiNfwmdfqdG4H6MA130_assertion wasDerivedFrom befree-20150227 NP1018342.RAAjWIkMdD_tS64pMAZsmW9KJ3l2GKiNfwmdfqdG4H6MA130_provenance.
- NP1018342.RAAjWIkMdD_tS64pMAZsmW9KJ3l2GKiNfwmdfqdG4H6MA130_assertion SIO_000772 16205833 NP1018342.RAAjWIkMdD_tS64pMAZsmW9KJ3l2GKiNfwmdfqdG4H6MA130_provenance.
- NP1018342.RAAjWIkMdD_tS64pMAZsmW9KJ3l2GKiNfwmdfqdG4H6MA130_assertion evidence source_evidence_literature NP1018342.RAAjWIkMdD_tS64pMAZsmW9KJ3l2GKiNfwmdfqdG4H6MA130_provenance.
- NP1018342.RAAjWIkMdD_tS64pMAZsmW9KJ3l2GKiNfwmdfqdG4H6MA130_assertion description "[Homocystinuria is an autosomal recessive inborn error of metabolism that is most often caused by mutation in the cystathionine beta-synthase (CBS) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1018342.RAAjWIkMdD_tS64pMAZsmW9KJ3l2GKiNfwmdfqdG4H6MA130_provenance.