Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP651070.RAxtLqHQuiZ9JvyGGRdjaFUeC6utmxJog4X9diE6lODi0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651070.RAxtLqHQuiZ9JvyGGRdjaFUeC6utmxJog4X9diE6lODi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651070.RAxtLqHQuiZ9JvyGGRdjaFUeC6utmxJog4X9diE6lODi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651070.RAxtLqHQuiZ9JvyGGRdjaFUeC6utmxJog4X9diE6lODi0130_provenance.
- NP651070.RAxtLqHQuiZ9JvyGGRdjaFUeC6utmxJog4X9diE6lODi0130_assertion description "[Autosomal dominant early-onset Alzheimer disease (EOAD) is a heterogeneous condition that has been associated with mutations in 3 different genes: the amyloid precursor protein (APP), presenilin 1 (PSEN1), and presenilin 2 (PSEN2) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651070.RAxtLqHQuiZ9JvyGGRdjaFUeC6utmxJog4X9diE6lODi0130_provenance.
- NP651070.RAxtLqHQuiZ9JvyGGRdjaFUeC6utmxJog4X9diE6lODi0130_assertion evidence source_evidence_literature NP651070.RAxtLqHQuiZ9JvyGGRdjaFUeC6utmxJog4X9diE6lODi0130_provenance.
- NP651070.RAxtLqHQuiZ9JvyGGRdjaFUeC6utmxJog4X9diE6lODi0130_assertion SIO_000772 19073399 NP651070.RAxtLqHQuiZ9JvyGGRdjaFUeC6utmxJog4X9diE6lODi0130_provenance.
- NP651070.RAxtLqHQuiZ9JvyGGRdjaFUeC6utmxJog4X9diE6lODi0130_assertion wasDerivedFrom befree-20150227 NP651070.RAxtLqHQuiZ9JvyGGRdjaFUeC6utmxJog4X9diE6lODi0130_provenance.
- NP651070.RAxtLqHQuiZ9JvyGGRdjaFUeC6utmxJog4X9diE6lODi0130_assertion wasGeneratedBy ECO_0000203 NP651070.RAxtLqHQuiZ9JvyGGRdjaFUeC6utmxJog4X9diE6lODi0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP651070.RAxtLqHQuiZ9JvyGGRdjaFUeC6utmxJog4X9diE6lODi0130_provenance.