Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP442112.RAsNr-V1WVtgF7Uxk_OKL2ORhSH9nPidXQVopiIdn4Jtg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP442112.RAsNr-V1WVtgF7Uxk_OKL2ORhSH9nPidXQVopiIdn4Jtg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP442112.RAsNr-V1WVtgF7Uxk_OKL2ORhSH9nPidXQVopiIdn4Jtg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP442112.RAsNr-V1WVtgF7Uxk_OKL2ORhSH9nPidXQVopiIdn4Jtg130_provenance.
- NP442112.RAsNr-V1WVtgF7Uxk_OKL2ORhSH9nPidXQVopiIdn4Jtg130_assertion description "[The most common histological variety was motor neurone disease type inclusion (MNDI) (n = 18), followed by corticobasal degeneration (CBD) (n = 12), then Pick's disease (n = 6), dementia lacking distinctive histology (DLDH) (n = 6) and PSP (n = 3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP442112.RAsNr-V1WVtgF7Uxk_OKL2ORhSH9nPidXQVopiIdn4Jtg130_provenance.
- NP442112.RAsNr-V1WVtgF7Uxk_OKL2ORhSH9nPidXQVopiIdn4Jtg130_assertion evidence source_evidence_literature NP442112.RAsNr-V1WVtgF7Uxk_OKL2ORhSH9nPidXQVopiIdn4Jtg130_provenance.
- NP442112.RAsNr-V1WVtgF7Uxk_OKL2ORhSH9nPidXQVopiIdn4Jtg130_assertion SIO_000772 16033782 NP442112.RAsNr-V1WVtgF7Uxk_OKL2ORhSH9nPidXQVopiIdn4Jtg130_provenance.
- NP442112.RAsNr-V1WVtgF7Uxk_OKL2ORhSH9nPidXQVopiIdn4Jtg130_assertion wasDerivedFrom befree-20140225 NP442112.RAsNr-V1WVtgF7Uxk_OKL2ORhSH9nPidXQVopiIdn4Jtg130_provenance.
- NP442112.RAsNr-V1WVtgF7Uxk_OKL2ORhSH9nPidXQVopiIdn4Jtg130_assertion wasGeneratedBy ECO_0000203 NP442112.RAsNr-V1WVtgF7Uxk_OKL2ORhSH9nPidXQVopiIdn4Jtg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP442112.RAsNr-V1WVtgF7Uxk_OKL2ORhSH9nPidXQVopiIdn4Jtg130_provenance.