Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418432.RAlUe9GSOq2E56x8YqOvPJoBPwi710n0ENqnfW4VTT0Aw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418432.RAlUe9GSOq2E56x8YqOvPJoBPwi710n0ENqnfW4VTT0Aw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418432.RAlUe9GSOq2E56x8YqOvPJoBPwi710n0ENqnfW4VTT0Aw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418432.RAlUe9GSOq2E56x8YqOvPJoBPwi710n0ENqnfW4VTT0Aw130_provenance.
- NP418432.RAlUe9GSOq2E56x8YqOvPJoBPwi710n0ENqnfW4VTT0Aw130_assertion description "[GlyRs formed from alpha 1R271K subunits showed a reduction of beta-alanine and taurine affinities and maximal inducible currents; the mutants alpha 1R271Q and alpha 1R271L associated with human hyperekplexia gave no responses to these ligands.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418432.RAlUe9GSOq2E56x8YqOvPJoBPwi710n0ENqnfW4VTT0Aw130_provenance.
- NP418432.RAlUe9GSOq2E56x8YqOvPJoBPwi710n0ENqnfW4VTT0Aw130_assertion evidence source_evidence_literature NP418432.RAlUe9GSOq2E56x8YqOvPJoBPwi710n0ENqnfW4VTT0Aw130_provenance.
- NP418432.RAlUe9GSOq2E56x8YqOvPJoBPwi710n0ENqnfW4VTT0Aw130_assertion SIO_000772 7542038 NP418432.RAlUe9GSOq2E56x8YqOvPJoBPwi710n0ENqnfW4VTT0Aw130_provenance.
- NP418432.RAlUe9GSOq2E56x8YqOvPJoBPwi710n0ENqnfW4VTT0Aw130_assertion wasDerivedFrom befree-20150227 NP418432.RAlUe9GSOq2E56x8YqOvPJoBPwi710n0ENqnfW4VTT0Aw130_provenance.
- NP418432.RAlUe9GSOq2E56x8YqOvPJoBPwi710n0ENqnfW4VTT0Aw130_assertion wasGeneratedBy ECO_0000203 NP418432.RAlUe9GSOq2E56x8YqOvPJoBPwi710n0ENqnfW4VTT0Aw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP418432.RAlUe9GSOq2E56x8YqOvPJoBPwi710n0ENqnfW4VTT0Aw130_provenance.