Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP959192.RAUrX2SuJoLgQbqjJBW4Iz6bpok3eZOiRDC9lUswHVXsk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP959192.RAUrX2SuJoLgQbqjJBW4Iz6bpok3eZOiRDC9lUswHVXsk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP959192.RAUrX2SuJoLgQbqjJBW4Iz6bpok3eZOiRDC9lUswHVXsk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP959192.RAUrX2SuJoLgQbqjJBW4Iz6bpok3eZOiRDC9lUswHVXsk130_provenance.
- NP959192.RAUrX2SuJoLgQbqjJBW4Iz6bpok3eZOiRDC9lUswHVXsk130_assertion description "[Pathogenic mutations in APP, PSEN1, PSEN2, MAPT and GRN have previously been linked to familial early onset forms of dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959192.RAUrX2SuJoLgQbqjJBW4Iz6bpok3eZOiRDC9lUswHVXsk130_provenance.
- NP959192.RAUrX2SuJoLgQbqjJBW4Iz6bpok3eZOiRDC9lUswHVXsk130_assertion evidence source_evidence_literature NP959192.RAUrX2SuJoLgQbqjJBW4Iz6bpok3eZOiRDC9lUswHVXsk130_provenance.
- NP959192.RAUrX2SuJoLgQbqjJBW4Iz6bpok3eZOiRDC9lUswHVXsk130_assertion SIO_000772 22312439 NP959192.RAUrX2SuJoLgQbqjJBW4Iz6bpok3eZOiRDC9lUswHVXsk130_provenance.
- NP959192.RAUrX2SuJoLgQbqjJBW4Iz6bpok3eZOiRDC9lUswHVXsk130_assertion wasDerivedFrom befree-2016 NP959192.RAUrX2SuJoLgQbqjJBW4Iz6bpok3eZOiRDC9lUswHVXsk130_provenance.
- NP959192.RAUrX2SuJoLgQbqjJBW4Iz6bpok3eZOiRDC9lUswHVXsk130_assertion wasGeneratedBy ECO_0000203 NP959192.RAUrX2SuJoLgQbqjJBW4Iz6bpok3eZOiRDC9lUswHVXsk130_provenance.
- befree-2016 importedOn "2016-02-19" NP959192.RAUrX2SuJoLgQbqjJBW4Iz6bpok3eZOiRDC9lUswHVXsk130_provenance.