Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP705683.RAfy8G1BmXeffkPw8x5bB0wIGX2mXGFAQPL6hccnEab9U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP705683.RAfy8G1BmXeffkPw8x5bB0wIGX2mXGFAQPL6hccnEab9U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP705683.RAfy8G1BmXeffkPw8x5bB0wIGX2mXGFAQPL6hccnEab9U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP705683.RAfy8G1BmXeffkPw8x5bB0wIGX2mXGFAQPL6hccnEab9U130_provenance.
- befree-2016 importedOn "2016-02-19" NP705683.RAfy8G1BmXeffkPw8x5bB0wIGX2mXGFAQPL6hccnEab9U130_provenance.
- NP705683.RAfy8G1BmXeffkPw8x5bB0wIGX2mXGFAQPL6hccnEab9U130_assertion wasGeneratedBy ECO_0000203 NP705683.RAfy8G1BmXeffkPw8x5bB0wIGX2mXGFAQPL6hccnEab9U130_provenance.
- NP705683.RAfy8G1BmXeffkPw8x5bB0wIGX2mXGFAQPL6hccnEab9U130_assertion wasDerivedFrom befree-2016 NP705683.RAfy8G1BmXeffkPw8x5bB0wIGX2mXGFAQPL6hccnEab9U130_provenance.
- NP705683.RAfy8G1BmXeffkPw8x5bB0wIGX2mXGFAQPL6hccnEab9U130_assertion SIO_000772 19033659 NP705683.RAfy8G1BmXeffkPw8x5bB0wIGX2mXGFAQPL6hccnEab9U130_provenance.
- NP705683.RAfy8G1BmXeffkPw8x5bB0wIGX2mXGFAQPL6hccnEab9U130_assertion evidence source_evidence_literature NP705683.RAfy8G1BmXeffkPw8x5bB0wIGX2mXGFAQPL6hccnEab9U130_provenance.
- NP705683.RAfy8G1BmXeffkPw8x5bB0wIGX2mXGFAQPL6hccnEab9U130_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." NP705683.RAfy8G1BmXeffkPw8x5bB0wIGX2mXGFAQPL6hccnEab9U130_provenance.