Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1294593.RADxvJ52V9L5GyxVf6qz271cu8ofzBiLUk5WsbWcoXmIo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1294593.RADxvJ52V9L5GyxVf6qz271cu8ofzBiLUk5WsbWcoXmIo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1294593.RADxvJ52V9L5GyxVf6qz271cu8ofzBiLUk5WsbWcoXmIo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1294593.RADxvJ52V9L5GyxVf6qz271cu8ofzBiLUk5WsbWcoXmIo130_provenance.
- NP1294593.RADxvJ52V9L5GyxVf6qz271cu8ofzBiLUk5WsbWcoXmIo130_assertion description "[We conclude that mutations in MAPT, including p.Q336H, can be associated with clinical, pathologic, and biochemical features that are similar to those in sporadic PiD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1294593.RADxvJ52V9L5GyxVf6qz271cu8ofzBiLUk5WsbWcoXmIo130_provenance.
- NP1294593.RADxvJ52V9L5GyxVf6qz271cu8ofzBiLUk5WsbWcoXmIo130_assertion evidence source_evidence_literature NP1294593.RADxvJ52V9L5GyxVf6qz271cu8ofzBiLUk5WsbWcoXmIo130_provenance.
- NP1294593.RADxvJ52V9L5GyxVf6qz271cu8ofzBiLUk5WsbWcoXmIo130_assertion SIO_000772 26426266 NP1294593.RADxvJ52V9L5GyxVf6qz271cu8ofzBiLUk5WsbWcoXmIo130_provenance.
- NP1294593.RADxvJ52V9L5GyxVf6qz271cu8ofzBiLUk5WsbWcoXmIo130_assertion wasDerivedFrom befree-2016 NP1294593.RADxvJ52V9L5GyxVf6qz271cu8ofzBiLUk5WsbWcoXmIo130_provenance.
- NP1294593.RADxvJ52V9L5GyxVf6qz271cu8ofzBiLUk5WsbWcoXmIo130_assertion wasGeneratedBy ECO_0000203 NP1294593.RADxvJ52V9L5GyxVf6qz271cu8ofzBiLUk5WsbWcoXmIo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1294593.RADxvJ52V9L5GyxVf6qz271cu8ofzBiLUk5WsbWcoXmIo130_provenance.