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- source_evidence_literature type ECO_0000212 NP260345.RAyhKI6V0o1tJxoJ-2mLEYfyOxlfX48xanR2Isn80RYjo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP260345.RAyhKI6V0o1tJxoJ-2mLEYfyOxlfX48xanR2Isn80RYjo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP260345.RAyhKI6V0o1tJxoJ-2mLEYfyOxlfX48xanR2Isn80RYjo130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP260345.RAyhKI6V0o1tJxoJ-2mLEYfyOxlfX48xanR2Isn80RYjo130_provenance.