Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP741932.RAoaKYWP9qMDRzqceBmZr6q5bOYojpEglP7xp_tE2l-_Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP741932.RAoaKYWP9qMDRzqceBmZr6q5bOYojpEglP7xp_tE2l-_Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP741932.RAoaKYWP9qMDRzqceBmZr6q5bOYojpEglP7xp_tE2l-_Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP741932.RAoaKYWP9qMDRzqceBmZr6q5bOYojpEglP7xp_tE2l-_Q130_provenance.
- NP741932.RAoaKYWP9qMDRzqceBmZr6q5bOYojpEglP7xp_tE2l-_Q130_assertion description "[Heritable mutations in the ttpA gene, encoding for TTP, result in ataxia with vitamin E deficiency (AVED) syndrome, typified by low vitamin E levels and a plethora of neurological disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP741932.RAoaKYWP9qMDRzqceBmZr6q5bOYojpEglP7xp_tE2l-_Q130_provenance.
- NP741932.RAoaKYWP9qMDRzqceBmZr6q5bOYojpEglP7xp_tE2l-_Q130_assertion evidence source_evidence_literature NP741932.RAoaKYWP9qMDRzqceBmZr6q5bOYojpEglP7xp_tE2l-_Q130_provenance.
- NP741932.RAoaKYWP9qMDRzqceBmZr6q5bOYojpEglP7xp_tE2l-_Q130_assertion SIO_000772 16819822 NP741932.RAoaKYWP9qMDRzqceBmZr6q5bOYojpEglP7xp_tE2l-_Q130_provenance.
- NP741932.RAoaKYWP9qMDRzqceBmZr6q5bOYojpEglP7xp_tE2l-_Q130_assertion wasDerivedFrom befree-20140225 NP741932.RAoaKYWP9qMDRzqceBmZr6q5bOYojpEglP7xp_tE2l-_Q130_provenance.
- NP741932.RAoaKYWP9qMDRzqceBmZr6q5bOYojpEglP7xp_tE2l-_Q130_assertion wasGeneratedBy ECO_0000203 NP741932.RAoaKYWP9qMDRzqceBmZr6q5bOYojpEglP7xp_tE2l-_Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP741932.RAoaKYWP9qMDRzqceBmZr6q5bOYojpEglP7xp_tE2l-_Q130_provenance.