Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_assertion> ?p ?o ?g. }
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- NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_assertion type Assertion NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_head.
- NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_assertion wasGeneratedBy ECO_0000203 NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_provenance.
- NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_assertion wasDerivedFrom befree-20140225 NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_provenance.
- NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_assertion SIO_000772 19033659 NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_provenance.
- NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_assertion evidence source_evidence_literature NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_provenance.
- NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_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." NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_provenance.