Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP838127.RAn3XtV9ymnapYTWrIJJeOK7MPcMs162P4J_p0Id2ZLmU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP838127.RAn3XtV9ymnapYTWrIJJeOK7MPcMs162P4J_p0Id2ZLmU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP838127.RAn3XtV9ymnapYTWrIJJeOK7MPcMs162P4J_p0Id2ZLmU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP838127.RAn3XtV9ymnapYTWrIJJeOK7MPcMs162P4J_p0Id2ZLmU130_provenance.
- NP838127.RAn3XtV9ymnapYTWrIJJeOK7MPcMs162P4J_p0Id2ZLmU130_assertion description "[Specifically, we will discuss how pathologies linked to the Dutch (E693Q) and Flemish AbetaPP (A692G) mutations have helped in understanding the role of CAA in dementia and in the development of dense-core plaques.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838127.RAn3XtV9ymnapYTWrIJJeOK7MPcMs162P4J_p0Id2ZLmU130_provenance.
- NP838127.RAn3XtV9ymnapYTWrIJJeOK7MPcMs162P4J_p0Id2ZLmU130_assertion evidence source_evidence_literature NP838127.RAn3XtV9ymnapYTWrIJJeOK7MPcMs162P4J_p0Id2ZLmU130_provenance.
- NP838127.RAn3XtV9ymnapYTWrIJJeOK7MPcMs162P4J_p0Id2ZLmU130_assertion SIO_000772 16914877 NP838127.RAn3XtV9ymnapYTWrIJJeOK7MPcMs162P4J_p0Id2ZLmU130_provenance.
- NP838127.RAn3XtV9ymnapYTWrIJJeOK7MPcMs162P4J_p0Id2ZLmU130_assertion wasDerivedFrom befree-20150227 NP838127.RAn3XtV9ymnapYTWrIJJeOK7MPcMs162P4J_p0Id2ZLmU130_provenance.
- NP838127.RAn3XtV9ymnapYTWrIJJeOK7MPcMs162P4J_p0Id2ZLmU130_assertion wasGeneratedBy ECO_0000203 NP838127.RAn3XtV9ymnapYTWrIJJeOK7MPcMs162P4J_p0Id2ZLmU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP838127.RAn3XtV9ymnapYTWrIJJeOK7MPcMs162P4J_p0Id2ZLmU130_provenance.