Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP563920.RAfklyhQ2yTmR6M_6eHCvImDP_am_KdRboyHx2Ml1-abA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP563920.RAfklyhQ2yTmR6M_6eHCvImDP_am_KdRboyHx2Ml1-abA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP563920.RAfklyhQ2yTmR6M_6eHCvImDP_am_KdRboyHx2Ml1-abA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP563920.RAfklyhQ2yTmR6M_6eHCvImDP_am_KdRboyHx2Ml1-abA130_provenance.
- NP563920.RAfklyhQ2yTmR6M_6eHCvImDP_am_KdRboyHx2Ml1-abA130_assertion wasGeneratedBy ECO_0000203 NP563920.RAfklyhQ2yTmR6M_6eHCvImDP_am_KdRboyHx2Ml1-abA130_provenance.
- NP563920.RAfklyhQ2yTmR6M_6eHCvImDP_am_KdRboyHx2Ml1-abA130_assertion wasDerivedFrom befree-20140225 NP563920.RAfklyhQ2yTmR6M_6eHCvImDP_am_KdRboyHx2Ml1-abA130_provenance.
- NP563920.RAfklyhQ2yTmR6M_6eHCvImDP_am_KdRboyHx2Ml1-abA130_assertion SIO_000772 19033659 NP563920.RAfklyhQ2yTmR6M_6eHCvImDP_am_KdRboyHx2Ml1-abA130_provenance.
- NP563920.RAfklyhQ2yTmR6M_6eHCvImDP_am_KdRboyHx2Ml1-abA130_assertion evidence source_evidence_literature NP563920.RAfklyhQ2yTmR6M_6eHCvImDP_am_KdRboyHx2Ml1-abA130_provenance.
- NP563920.RAfklyhQ2yTmR6M_6eHCvImDP_am_KdRboyHx2Ml1-abA130_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." NP563920.RAfklyhQ2yTmR6M_6eHCvImDP_am_KdRboyHx2Ml1-abA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP563920.RAfklyhQ2yTmR6M_6eHCvImDP_am_KdRboyHx2Ml1-abA130_provenance.