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- source_evidence_literature type ECO_0000212 NP428629.RA2mRxc5jukdk5L50--8Nxvwzc6Ekup5fABCVotMOxMsY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP428629.RA2mRxc5jukdk5L50--8Nxvwzc6Ekup5fABCVotMOxMsY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP428629.RA2mRxc5jukdk5L50--8Nxvwzc6Ekup5fABCVotMOxMsY130_provenance.
- NP428629.RA2mRxc5jukdk5L50--8Nxvwzc6Ekup5fABCVotMOxMsY130_assertion description "[The percentage of involved Chinese families with autosomal dominant hereditary spastic paraplegia with an SPG4 mutation is 18% (4/22), lower than the estimated 40% linked to this locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428629.RA2mRxc5jukdk5L50--8Nxvwzc6Ekup5fABCVotMOxMsY130_provenance.
- NP428629.RA2mRxc5jukdk5L50--8Nxvwzc6Ekup5fABCVotMOxMsY130_assertion evidence source_evidence_literature NP428629.RA2mRxc5jukdk5L50--8Nxvwzc6Ekup5fABCVotMOxMsY130_provenance.
- NP428629.RA2mRxc5jukdk5L50--8Nxvwzc6Ekup5fABCVotMOxMsY130_assertion SIO_000772 14732620 NP428629.RA2mRxc5jukdk5L50--8Nxvwzc6Ekup5fABCVotMOxMsY130_provenance.
- NP428629.RA2mRxc5jukdk5L50--8Nxvwzc6Ekup5fABCVotMOxMsY130_assertion wasDerivedFrom befree-2016 NP428629.RA2mRxc5jukdk5L50--8Nxvwzc6Ekup5fABCVotMOxMsY130_provenance.
- NP428629.RA2mRxc5jukdk5L50--8Nxvwzc6Ekup5fABCVotMOxMsY130_assertion wasGeneratedBy ECO_0000203 NP428629.RA2mRxc5jukdk5L50--8Nxvwzc6Ekup5fABCVotMOxMsY130_provenance.
- befree-2016 importedOn "2016-02-19" NP428629.RA2mRxc5jukdk5L50--8Nxvwzc6Ekup5fABCVotMOxMsY130_provenance.