Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP968492.RAHK7XQGON_yb5qSuKwurdrU6W9c9E6zmhX9rTAZYngcI130_assertion> ?p ?o ?g. }
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- NP968492.RAHK7XQGON_yb5qSuKwurdrU6W9c9E6zmhX9rTAZYngcI130_assertion type Assertion NP968492.RAHK7XQGON_yb5qSuKwurdrU6W9c9E6zmhX9rTAZYngcI130_head.
- NP968492.RAHK7XQGON_yb5qSuKwurdrU6W9c9E6zmhX9rTAZYngcI130_assertion wasGeneratedBy ECO_0000203 NP968492.RAHK7XQGON_yb5qSuKwurdrU6W9c9E6zmhX9rTAZYngcI130_provenance.
- NP968492.RAHK7XQGON_yb5qSuKwurdrU6W9c9E6zmhX9rTAZYngcI130_assertion wasDerivedFrom befree-20150227 NP968492.RAHK7XQGON_yb5qSuKwurdrU6W9c9E6zmhX9rTAZYngcI130_provenance.
- NP968492.RAHK7XQGON_yb5qSuKwurdrU6W9c9E6zmhX9rTAZYngcI130_assertion SIO_000772 19033659 NP968492.RAHK7XQGON_yb5qSuKwurdrU6W9c9E6zmhX9rTAZYngcI130_provenance.
- NP968492.RAHK7XQGON_yb5qSuKwurdrU6W9c9E6zmhX9rTAZYngcI130_assertion evidence source_evidence_literature NP968492.RAHK7XQGON_yb5qSuKwurdrU6W9c9E6zmhX9rTAZYngcI130_provenance.
- NP968492.RAHK7XQGON_yb5qSuKwurdrU6W9c9E6zmhX9rTAZYngcI130_assertion description "[Additional mutations were identified in the genes encoding the putative glycine transporter SLC6A18 (XT2) and the neutral amino acid transporter SLC6A19 (B0AT1) in families with either IG or HG, suggesting that mutations in the genes encoding these transporters may also contribute to these phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP968492.RAHK7XQGON_yb5qSuKwurdrU6W9c9E6zmhX9rTAZYngcI130_provenance.