Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP8554.RAiw1Pc6Ev_1rkZ6qIM_Qf8s2aZtgFLroMtxsJaWVf3G4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP8554.RAiw1Pc6Ev_1rkZ6qIM_Qf8s2aZtgFLroMtxsJaWVf3G4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8554.RAiw1Pc6Ev_1rkZ6qIM_Qf8s2aZtgFLroMtxsJaWVf3G4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8554.RAiw1Pc6Ev_1rkZ6qIM_Qf8s2aZtgFLroMtxsJaWVf3G4130_provenance.
- NP8554.RAiw1Pc6Ev_1rkZ6qIM_Qf8s2aZtgFLroMtxsJaWVf3G4130_assertion description "[Missense mutations are frequent in the gene for X-chromosomal adrenoleukodystrophy (ALD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8554.RAiw1Pc6Ev_1rkZ6qIM_Qf8s2aZtgFLroMtxsJaWVf3G4130_provenance.
- NP8554.RAiw1Pc6Ev_1rkZ6qIM_Qf8s2aZtgFLroMtxsJaWVf3G4130_assertion evidence source_evidence_curated NP8554.RAiw1Pc6Ev_1rkZ6qIM_Qf8s2aZtgFLroMtxsJaWVf3G4130_provenance.
- NP8554.RAiw1Pc6Ev_1rkZ6qIM_Qf8s2aZtgFLroMtxsJaWVf3G4130_assertion SIO_000772 7849723 NP8554.RAiw1Pc6Ev_1rkZ6qIM_Qf8s2aZtgFLroMtxsJaWVf3G4130_provenance.
- NP8554.RAiw1Pc6Ev_1rkZ6qIM_Qf8s2aZtgFLroMtxsJaWVf3G4130_assertion wasDerivedFrom uniprot-2016 NP8554.RAiw1Pc6Ev_1rkZ6qIM_Qf8s2aZtgFLroMtxsJaWVf3G4130_provenance.
- NP8554.RAiw1Pc6Ev_1rkZ6qIM_Qf8s2aZtgFLroMtxsJaWVf3G4130_assertion wasGeneratedBy ECO_0000218 NP8554.RAiw1Pc6Ev_1rkZ6qIM_Qf8s2aZtgFLroMtxsJaWVf3G4130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP8554.RAiw1Pc6Ev_1rkZ6qIM_Qf8s2aZtgFLroMtxsJaWVf3G4130_provenance.