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- source_evidence_literature type ECO_0000212 NP1311613.RA5GP1zFwoPosj8u8B3WaMpiOiIp_buWWsvy3b2kkSX0o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1311613.RA5GP1zFwoPosj8u8B3WaMpiOiIp_buWWsvy3b2kkSX0o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1311613.RA5GP1zFwoPosj8u8B3WaMpiOiIp_buWWsvy3b2kkSX0o130_provenance.
- NP1311613.RA5GP1zFwoPosj8u8B3WaMpiOiIp_buWWsvy3b2kkSX0o130_assertion description "[Abnormalities of peripheral myelin protein 22 (PMP-22) account for dominantly inherited HMSN type I in approximately 90% of families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1311613.RA5GP1zFwoPosj8u8B3WaMpiOiIp_buWWsvy3b2kkSX0o130_provenance.
- NP1311613.RA5GP1zFwoPosj8u8B3WaMpiOiIp_buWWsvy3b2kkSX0o130_assertion evidence source_evidence_literature NP1311613.RA5GP1zFwoPosj8u8B3WaMpiOiIp_buWWsvy3b2kkSX0o130_provenance.
- NP1311613.RA5GP1zFwoPosj8u8B3WaMpiOiIp_buWWsvy3b2kkSX0o130_assertion SIO_000772 7541290 NP1311613.RA5GP1zFwoPosj8u8B3WaMpiOiIp_buWWsvy3b2kkSX0o130_provenance.
- NP1311613.RA5GP1zFwoPosj8u8B3WaMpiOiIp_buWWsvy3b2kkSX0o130_assertion wasDerivedFrom befree-2016 NP1311613.RA5GP1zFwoPosj8u8B3WaMpiOiIp_buWWsvy3b2kkSX0o130_provenance.
- NP1311613.RA5GP1zFwoPosj8u8B3WaMpiOiIp_buWWsvy3b2kkSX0o130_assertion wasGeneratedBy ECO_0000203 NP1311613.RA5GP1zFwoPosj8u8B3WaMpiOiIp_buWWsvy3b2kkSX0o130_provenance.
- befree-2016 importedOn "2016-02-19" NP1311613.RA5GP1zFwoPosj8u8B3WaMpiOiIp_buWWsvy3b2kkSX0o130_provenance.