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- NP260345.RAyhKI6V0o1tJxoJ-2mLEYfyOxlfX48xanR2Isn80RYjo130_assertion type Assertion NP260345.RAyhKI6V0o1tJxoJ-2mLEYfyOxlfX48xanR2Isn80RYjo130_head.
- NP260345.RAyhKI6V0o1tJxoJ-2mLEYfyOxlfX48xanR2Isn80RYjo130_assertion description "[Identification of a common PEX1 mutation in Zellweger syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP260345.RAyhKI6V0o1tJxoJ-2mLEYfyOxlfX48xanR2Isn80RYjo130_provenance.
- NP260345.RAyhKI6V0o1tJxoJ-2mLEYfyOxlfX48xanR2Isn80RYjo130_assertion evidence source_evidence_literature NP260345.RAyhKI6V0o1tJxoJ-2mLEYfyOxlfX48xanR2Isn80RYjo130_provenance.
- NP260345.RAyhKI6V0o1tJxoJ-2mLEYfyOxlfX48xanR2Isn80RYjo130_assertion SIO_000772 10447258 NP260345.RAyhKI6V0o1tJxoJ-2mLEYfyOxlfX48xanR2Isn80RYjo130_provenance.
- NP260345.RAyhKI6V0o1tJxoJ-2mLEYfyOxlfX48xanR2Isn80RYjo130_assertion wasDerivedFrom befree-2016 NP260345.RAyhKI6V0o1tJxoJ-2mLEYfyOxlfX48xanR2Isn80RYjo130_provenance.
- NP260345.RAyhKI6V0o1tJxoJ-2mLEYfyOxlfX48xanR2Isn80RYjo130_assertion wasGeneratedBy ECO_0000203 NP260345.RAyhKI6V0o1tJxoJ-2mLEYfyOxlfX48xanR2Isn80RYjo130_provenance.