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- NP286749.RA-FAagNIJrS8NaQSWuGnVXbgF4aBP35gTPBdnwi2nID8130_assertion type Assertion NP286749.RA-FAagNIJrS8NaQSWuGnVXbgF4aBP35gTPBdnwi2nID8130_head.
- NP286749.RA-FAagNIJrS8NaQSWuGnVXbgF4aBP35gTPBdnwi2nID8130_assertion wasGeneratedBy ECO_0000203 NP286749.RA-FAagNIJrS8NaQSWuGnVXbgF4aBP35gTPBdnwi2nID8130_provenance.
- NP286749.RA-FAagNIJrS8NaQSWuGnVXbgF4aBP35gTPBdnwi2nID8130_assertion wasDerivedFrom befree-20150227 NP286749.RA-FAagNIJrS8NaQSWuGnVXbgF4aBP35gTPBdnwi2nID8130_provenance.
- NP286749.RA-FAagNIJrS8NaQSWuGnVXbgF4aBP35gTPBdnwi2nID8130_assertion SIO_000772 16205833 NP286749.RA-FAagNIJrS8NaQSWuGnVXbgF4aBP35gTPBdnwi2nID8130_provenance.
- NP286749.RA-FAagNIJrS8NaQSWuGnVXbgF4aBP35gTPBdnwi2nID8130_assertion evidence source_evidence_literature NP286749.RA-FAagNIJrS8NaQSWuGnVXbgF4aBP35gTPBdnwi2nID8130_provenance.
- NP286749.RA-FAagNIJrS8NaQSWuGnVXbgF4aBP35gTPBdnwi2nID8130_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." NP286749.RA-FAagNIJrS8NaQSWuGnVXbgF4aBP35gTPBdnwi2nID8130_provenance.