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- NP741474.RAnpjuq0KFKRZVviNejCq2JYVd_i0gAf4U52aAymf7hJo130_assertion type Assertion NP741474.RAnpjuq0KFKRZVviNejCq2JYVd_i0gAf4U52aAymf7hJo130_head.
- NP741474.RAnpjuq0KFKRZVviNejCq2JYVd_i0gAf4U52aAymf7hJo130_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." NP741474.RAnpjuq0KFKRZVviNejCq2JYVd_i0gAf4U52aAymf7hJo130_provenance.
- NP741474.RAnpjuq0KFKRZVviNejCq2JYVd_i0gAf4U52aAymf7hJo130_assertion evidence source_evidence_literature NP741474.RAnpjuq0KFKRZVviNejCq2JYVd_i0gAf4U52aAymf7hJo130_provenance.
- NP741474.RAnpjuq0KFKRZVviNejCq2JYVd_i0gAf4U52aAymf7hJo130_assertion SIO_000772 16205833 NP741474.RAnpjuq0KFKRZVviNejCq2JYVd_i0gAf4U52aAymf7hJo130_provenance.
- NP741474.RAnpjuq0KFKRZVviNejCq2JYVd_i0gAf4U52aAymf7hJo130_assertion wasDerivedFrom befree-20140225 NP741474.RAnpjuq0KFKRZVviNejCq2JYVd_i0gAf4U52aAymf7hJo130_provenance.
- NP741474.RAnpjuq0KFKRZVviNejCq2JYVd_i0gAf4U52aAymf7hJo130_assertion wasGeneratedBy ECO_0000203 NP741474.RAnpjuq0KFKRZVviNejCq2JYVd_i0gAf4U52aAymf7hJo130_provenance.