Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP427308.RAbz6V_7xI0vRhm1_VqP6WyT1IBu69HfbZ0SmiUDLUQys130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP427308.RAbz6V_7xI0vRhm1_VqP6WyT1IBu69HfbZ0SmiUDLUQys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP427308.RAbz6V_7xI0vRhm1_VqP6WyT1IBu69HfbZ0SmiUDLUQys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP427308.RAbz6V_7xI0vRhm1_VqP6WyT1IBu69HfbZ0SmiUDLUQys130_provenance.
- NP427308.RAbz6V_7xI0vRhm1_VqP6WyT1IBu69HfbZ0SmiUDLUQys130_assertion description "[The defect, however, is different from I-cell disease and pseudo-Hurler polydystrophy, two disorders of post-translational lysosomal enzyme biosynthesis, since complementation studies demonstrated recovery of intracellular beta-galactosidase and alpha-neuraminidase levels in heterokaryons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427308.RAbz6V_7xI0vRhm1_VqP6WyT1IBu69HfbZ0SmiUDLUQys130_provenance.
- NP427308.RAbz6V_7xI0vRhm1_VqP6WyT1IBu69HfbZ0SmiUDLUQys130_assertion evidence source_evidence_literature NP427308.RAbz6V_7xI0vRhm1_VqP6WyT1IBu69HfbZ0SmiUDLUQys130_provenance.
- NP427308.RAbz6V_7xI0vRhm1_VqP6WyT1IBu69HfbZ0SmiUDLUQys130_assertion SIO_000772 7076257 NP427308.RAbz6V_7xI0vRhm1_VqP6WyT1IBu69HfbZ0SmiUDLUQys130_provenance.
- NP427308.RAbz6V_7xI0vRhm1_VqP6WyT1IBu69HfbZ0SmiUDLUQys130_assertion wasDerivedFrom befree-20150227 NP427308.RAbz6V_7xI0vRhm1_VqP6WyT1IBu69HfbZ0SmiUDLUQys130_provenance.
- NP427308.RAbz6V_7xI0vRhm1_VqP6WyT1IBu69HfbZ0SmiUDLUQys130_assertion wasGeneratedBy ECO_0000203 NP427308.RAbz6V_7xI0vRhm1_VqP6WyT1IBu69HfbZ0SmiUDLUQys130_provenance.
- befree-20150227 importedOn "2015-02-27" NP427308.RAbz6V_7xI0vRhm1_VqP6WyT1IBu69HfbZ0SmiUDLUQys130_provenance.