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- NP276857.RABDii6ELtrHwtwPVIMR-WIlyQFrw-75WKD0s6Me_uWiI130_assertion type Assertion NP276857.RABDii6ELtrHwtwPVIMR-WIlyQFrw-75WKD0s6Me_uWiI130_head.
- NP276857.RABDii6ELtrHwtwPVIMR-WIlyQFrw-75WKD0s6Me_uWiI130_assertion wasGeneratedBy ECO_0000203 NP276857.RABDii6ELtrHwtwPVIMR-WIlyQFrw-75WKD0s6Me_uWiI130_provenance.
- NP276857.RABDii6ELtrHwtwPVIMR-WIlyQFrw-75WKD0s6Me_uWiI130_assertion wasDerivedFrom befree-2016 NP276857.RABDii6ELtrHwtwPVIMR-WIlyQFrw-75WKD0s6Me_uWiI130_provenance.
- NP276857.RABDii6ELtrHwtwPVIMR-WIlyQFrw-75WKD0s6Me_uWiI130_assertion SIO_000772 10699187 NP276857.RABDii6ELtrHwtwPVIMR-WIlyQFrw-75WKD0s6Me_uWiI130_provenance.
- NP276857.RABDii6ELtrHwtwPVIMR-WIlyQFrw-75WKD0s6Me_uWiI130_assertion evidence source_evidence_literature NP276857.RABDii6ELtrHwtwPVIMR-WIlyQFrw-75WKD0s6Me_uWiI130_provenance.
- NP276857.RABDii6ELtrHwtwPVIMR-WIlyQFrw-75WKD0s6Me_uWiI130_assertion description "[Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276857.RABDii6ELtrHwtwPVIMR-WIlyQFrw-75WKD0s6Me_uWiI130_provenance.