Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP3569.RAJNi5rqb-v2bPOIfkxN45EJvR6BnVaw2WDsM9IBnY0zI130_assertion> ?p ?o ?g. }
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- NP3569.RAJNi5rqb-v2bPOIfkxN45EJvR6BnVaw2WDsM9IBnY0zI130_assertion type Assertion NP3569.RAJNi5rqb-v2bPOIfkxN45EJvR6BnVaw2WDsM9IBnY0zI130_head.
- NP3569.RAJNi5rqb-v2bPOIfkxN45EJvR6BnVaw2WDsM9IBnY0zI130_assertion description "[Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3569.RAJNi5rqb-v2bPOIfkxN45EJvR6BnVaw2WDsM9IBnY0zI130_provenance.
- NP3569.RAJNi5rqb-v2bPOIfkxN45EJvR6BnVaw2WDsM9IBnY0zI130_assertion evidence source_evidence_curated NP3569.RAJNi5rqb-v2bPOIfkxN45EJvR6BnVaw2WDsM9IBnY0zI130_provenance.
- NP3569.RAJNi5rqb-v2bPOIfkxN45EJvR6BnVaw2WDsM9IBnY0zI130_assertion SIO_000772 15286787 NP3569.RAJNi5rqb-v2bPOIfkxN45EJvR6BnVaw2WDsM9IBnY0zI130_provenance.
- NP3569.RAJNi5rqb-v2bPOIfkxN45EJvR6BnVaw2WDsM9IBnY0zI130_assertion wasDerivedFrom uniprot-2016 NP3569.RAJNi5rqb-v2bPOIfkxN45EJvR6BnVaw2WDsM9IBnY0zI130_provenance.
- NP3569.RAJNi5rqb-v2bPOIfkxN45EJvR6BnVaw2WDsM9IBnY0zI130_assertion wasGeneratedBy ECO_0000218 NP3569.RAJNi5rqb-v2bPOIfkxN45EJvR6BnVaw2WDsM9IBnY0zI130_provenance.