Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP65825.RAlxIyIN6NfgVJCDSZ1h-Xt099GsyLpPzysHTIV4OCteo130_assertion> ?p ?o ?g. }
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- NP65825.RAlxIyIN6NfgVJCDSZ1h-Xt099GsyLpPzysHTIV4OCteo130_assertion type Assertion NP65825.RAlxIyIN6NfgVJCDSZ1h-Xt099GsyLpPzysHTIV4OCteo130_head.
- NP65825.RAlxIyIN6NfgVJCDSZ1h-Xt099GsyLpPzysHTIV4OCteo130_assertion wasGeneratedBy ECO_0000203 NP65825.RAlxIyIN6NfgVJCDSZ1h-Xt099GsyLpPzysHTIV4OCteo130_provenance.
- NP65825.RAlxIyIN6NfgVJCDSZ1h-Xt099GsyLpPzysHTIV4OCteo130_assertion wasDerivedFrom gad-20150221 NP65825.RAlxIyIN6NfgVJCDSZ1h-Xt099GsyLpPzysHTIV4OCteo130_provenance.
- NP65825.RAlxIyIN6NfgVJCDSZ1h-Xt099GsyLpPzysHTIV4OCteo130_assertion SIO_000772 19657220 NP65825.RAlxIyIN6NfgVJCDSZ1h-Xt099GsyLpPzysHTIV4OCteo130_provenance.
- NP65825.RAlxIyIN6NfgVJCDSZ1h-Xt099GsyLpPzysHTIV4OCteo130_assertion evidence source_evidence_literature NP65825.RAlxIyIN6NfgVJCDSZ1h-Xt099GsyLpPzysHTIV4OCteo130_provenance.
- NP65825.RAlxIyIN6NfgVJCDSZ1h-Xt099GsyLpPzysHTIV4OCteo130_assertion description "[The percentage of N29I mutations in ACP patients was higher than that reported in other studies, while the percentage of N34S and AAT mutations in ACP and idiopathic CP patients was similar.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65825.RAlxIyIN6NfgVJCDSZ1h-Xt099GsyLpPzysHTIV4OCteo130_provenance.