Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1006226.RAlO48g_-IOLWLTqaQvw-aZFm3x3LnL55UqALSf1RkrM8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1006226.RAlO48g_-IOLWLTqaQvw-aZFm3x3LnL55UqALSf1RkrM8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1006226.RAlO48g_-IOLWLTqaQvw-aZFm3x3LnL55UqALSf1RkrM8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1006226.RAlO48g_-IOLWLTqaQvw-aZFm3x3LnL55UqALSf1RkrM8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1006226.RAlO48g_-IOLWLTqaQvw-aZFm3x3LnL55UqALSf1RkrM8130_provenance.
- NP1006226.RAlO48g_-IOLWLTqaQvw-aZFm3x3LnL55UqALSf1RkrM8130_assertion wasGeneratedBy ECO_0000203 NP1006226.RAlO48g_-IOLWLTqaQvw-aZFm3x3LnL55UqALSf1RkrM8130_provenance.
- NP1006226.RAlO48g_-IOLWLTqaQvw-aZFm3x3LnL55UqALSf1RkrM8130_assertion wasDerivedFrom befree-20150227 NP1006226.RAlO48g_-IOLWLTqaQvw-aZFm3x3LnL55UqALSf1RkrM8130_provenance.
- NP1006226.RAlO48g_-IOLWLTqaQvw-aZFm3x3LnL55UqALSf1RkrM8130_assertion SIO_000772 18818286 NP1006226.RAlO48g_-IOLWLTqaQvw-aZFm3x3LnL55UqALSf1RkrM8130_provenance.
- NP1006226.RAlO48g_-IOLWLTqaQvw-aZFm3x3LnL55UqALSf1RkrM8130_assertion evidence source_evidence_literature NP1006226.RAlO48g_-IOLWLTqaQvw-aZFm3x3LnL55UqALSf1RkrM8130_provenance.
- NP1006226.RAlO48g_-IOLWLTqaQvw-aZFm3x3LnL55UqALSf1RkrM8130_assertion description "[Combination of models of familial AD that develop severe amyloidosis with those displaying defects in insulin/IGF-I signaling may help clarify the link between putative initial metabolic disturbances and mechanisms of pathological progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1006226.RAlO48g_-IOLWLTqaQvw-aZFm3x3LnL55UqALSf1RkrM8130_provenance.