Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP226814.RAD7PQov6oLY2wBg3ywTKE6u99DnxoZZwEBMYqVawZNc8130_assertion> ?p ?o ?g. }
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- NP226814.RAD7PQov6oLY2wBg3ywTKE6u99DnxoZZwEBMYqVawZNc8130_assertion type Assertion NP226814.RAD7PQov6oLY2wBg3ywTKE6u99DnxoZZwEBMYqVawZNc8130_head.
- NP226814.RAD7PQov6oLY2wBg3ywTKE6u99DnxoZZwEBMYqVawZNc8130_assertion description "[Deficiency in hepatic tyrosine aminotransferase (TAT) causes tyrosinemia type II, an autosomal recessively inherited disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226814.RAD7PQov6oLY2wBg3ywTKE6u99DnxoZZwEBMYqVawZNc8130_provenance.
- NP226814.RAD7PQov6oLY2wBg3ywTKE6u99DnxoZZwEBMYqVawZNc8130_assertion evidence source_evidence_literature NP226814.RAD7PQov6oLY2wBg3ywTKE6u99DnxoZZwEBMYqVawZNc8130_provenance.
- NP226814.RAD7PQov6oLY2wBg3ywTKE6u99DnxoZZwEBMYqVawZNc8130_assertion SIO_000772 2456982 NP226814.RAD7PQov6oLY2wBg3ywTKE6u99DnxoZZwEBMYqVawZNc8130_provenance.
- NP226814.RAD7PQov6oLY2wBg3ywTKE6u99DnxoZZwEBMYqVawZNc8130_assertion wasDerivedFrom befree-20140225 NP226814.RAD7PQov6oLY2wBg3ywTKE6u99DnxoZZwEBMYqVawZNc8130_provenance.
- NP226814.RAD7PQov6oLY2wBg3ywTKE6u99DnxoZZwEBMYqVawZNc8130_assertion wasGeneratedBy ECO_0000203 NP226814.RAD7PQov6oLY2wBg3ywTKE6u99DnxoZZwEBMYqVawZNc8130_provenance.