Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP247020.RAPrC5VmU0u3YHsoGmtyF2yT2jZ0g6EHr4yCCjEFFSLpw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP247020.RAPrC5VmU0u3YHsoGmtyF2yT2jZ0g6EHr4yCCjEFFSLpw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP247020.RAPrC5VmU0u3YHsoGmtyF2yT2jZ0g6EHr4yCCjEFFSLpw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP247020.RAPrC5VmU0u3YHsoGmtyF2yT2jZ0g6EHr4yCCjEFFSLpw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP247020.RAPrC5VmU0u3YHsoGmtyF2yT2jZ0g6EHr4yCCjEFFSLpw130_provenance.
- NP247020.RAPrC5VmU0u3YHsoGmtyF2yT2jZ0g6EHr4yCCjEFFSLpw130_assertion wasGeneratedBy ECO_0000203 NP247020.RAPrC5VmU0u3YHsoGmtyF2yT2jZ0g6EHr4yCCjEFFSLpw130_provenance.
- NP247020.RAPrC5VmU0u3YHsoGmtyF2yT2jZ0g6EHr4yCCjEFFSLpw130_assertion wasDerivedFrom befree-20150227 NP247020.RAPrC5VmU0u3YHsoGmtyF2yT2jZ0g6EHr4yCCjEFFSLpw130_provenance.
- NP247020.RAPrC5VmU0u3YHsoGmtyF2yT2jZ0g6EHr4yCCjEFFSLpw130_assertion SIO_000772 23931937 NP247020.RAPrC5VmU0u3YHsoGmtyF2yT2jZ0g6EHr4yCCjEFFSLpw130_provenance.
- NP247020.RAPrC5VmU0u3YHsoGmtyF2yT2jZ0g6EHr4yCCjEFFSLpw130_assertion evidence source_evidence_literature NP247020.RAPrC5VmU0u3YHsoGmtyF2yT2jZ0g6EHr4yCCjEFFSLpw130_provenance.
- NP247020.RAPrC5VmU0u3YHsoGmtyF2yT2jZ0g6EHr4yCCjEFFSLpw130_assertion description "[We report a novel missense mutation, D678H, in the APP gene in a Taiwanese patient who had progressive cognitive decline beginning in middle age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP247020.RAPrC5VmU0u3YHsoGmtyF2yT2jZ0g6EHr4yCCjEFFSLpw130_provenance.