Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP985735.RAOoqNbw5n5EI8_vTSEuo5oLgwcRTi7TWK3YIDJAlmPds130_assertion> ?p ?o ?g. }
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- NP985735.RAOoqNbw5n5EI8_vTSEuo5oLgwcRTi7TWK3YIDJAlmPds130_assertion type Assertion NP985735.RAOoqNbw5n5EI8_vTSEuo5oLgwcRTi7TWK3YIDJAlmPds130_head.
- NP985735.RAOoqNbw5n5EI8_vTSEuo5oLgwcRTi7TWK3YIDJAlmPds130_assertion wasGeneratedBy ECO_0000203 NP985735.RAOoqNbw5n5EI8_vTSEuo5oLgwcRTi7TWK3YIDJAlmPds130_provenance.
- NP985735.RAOoqNbw5n5EI8_vTSEuo5oLgwcRTi7TWK3YIDJAlmPds130_assertion wasDerivedFrom befree-20150227 NP985735.RAOoqNbw5n5EI8_vTSEuo5oLgwcRTi7TWK3YIDJAlmPds130_provenance.
- NP985735.RAOoqNbw5n5EI8_vTSEuo5oLgwcRTi7TWK3YIDJAlmPds130_assertion SIO_000772 19033659 NP985735.RAOoqNbw5n5EI8_vTSEuo5oLgwcRTi7TWK3YIDJAlmPds130_provenance.
- NP985735.RAOoqNbw5n5EI8_vTSEuo5oLgwcRTi7TWK3YIDJAlmPds130_assertion evidence source_evidence_literature NP985735.RAOoqNbw5n5EI8_vTSEuo5oLgwcRTi7TWK3YIDJAlmPds130_provenance.
- NP985735.RAOoqNbw5n5EI8_vTSEuo5oLgwcRTi7TWK3YIDJAlmPds130_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." NP985735.RAOoqNbw5n5EI8_vTSEuo5oLgwcRTi7TWK3YIDJAlmPds130_provenance.