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- source_evidence_literature type ECO_0000212 NP642371.RA3R1kiYz3aXmH1wYF0GOYjpK_B8P0qhQWIITl2bEUwIM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP642371.RA3R1kiYz3aXmH1wYF0GOYjpK_B8P0qhQWIITl2bEUwIM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP642371.RA3R1kiYz3aXmH1wYF0GOYjpK_B8P0qhQWIITl2bEUwIM130_provenance.
- NP642371.RA3R1kiYz3aXmH1wYF0GOYjpK_B8P0qhQWIITl2bEUwIM130_assertion description "[Identification of the genes that are mutated in genetic diseases characterized by the development of either neurofibromas and MPNSTs [neurofibromatosis type 1 (NF1)] or schwannomas [neurofibromatosis type 2 (NF2), schwannomatosis and Carney complex type 1] has greatly advanced our understanding of these mechanisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642371.RA3R1kiYz3aXmH1wYF0GOYjpK_B8P0qhQWIITl2bEUwIM130_provenance.
- NP642371.RA3R1kiYz3aXmH1wYF0GOYjpK_B8P0qhQWIITl2bEUwIM130_assertion evidence source_evidence_literature NP642371.RA3R1kiYz3aXmH1wYF0GOYjpK_B8P0qhQWIITl2bEUwIM130_provenance.
- NP642371.RA3R1kiYz3aXmH1wYF0GOYjpK_B8P0qhQWIITl2bEUwIM130_assertion SIO_000772 22160322 NP642371.RA3R1kiYz3aXmH1wYF0GOYjpK_B8P0qhQWIITl2bEUwIM130_provenance.
- NP642371.RA3R1kiYz3aXmH1wYF0GOYjpK_B8P0qhQWIITl2bEUwIM130_assertion wasDerivedFrom befree-20150227 NP642371.RA3R1kiYz3aXmH1wYF0GOYjpK_B8P0qhQWIITl2bEUwIM130_provenance.
- NP642371.RA3R1kiYz3aXmH1wYF0GOYjpK_B8P0qhQWIITl2bEUwIM130_assertion wasGeneratedBy ECO_0000203 NP642371.RA3R1kiYz3aXmH1wYF0GOYjpK_B8P0qhQWIITl2bEUwIM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP642371.RA3R1kiYz3aXmH1wYF0GOYjpK_B8P0qhQWIITl2bEUwIM130_provenance.