Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP14868.RAQYxkQt4w2sT-76EEOLPCdpoaLO3sGlnE3QH_P8NFKGs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP14868.RAQYxkQt4w2sT-76EEOLPCdpoaLO3sGlnE3QH_P8NFKGs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP14868.RAQYxkQt4w2sT-76EEOLPCdpoaLO3sGlnE3QH_P8NFKGs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP14868.RAQYxkQt4w2sT-76EEOLPCdpoaLO3sGlnE3QH_P8NFKGs130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP14868.RAQYxkQt4w2sT-76EEOLPCdpoaLO3sGlnE3QH_P8NFKGs130_provenance.
- NP14868.RAQYxkQt4w2sT-76EEOLPCdpoaLO3sGlnE3QH_P8NFKGs130_assertion wasGeneratedBy ECO_0000218 NP14868.RAQYxkQt4w2sT-76EEOLPCdpoaLO3sGlnE3QH_P8NFKGs130_provenance.
- NP14868.RAQYxkQt4w2sT-76EEOLPCdpoaLO3sGlnE3QH_P8NFKGs130_assertion wasDerivedFrom ctd_human-20150221 NP14868.RAQYxkQt4w2sT-76EEOLPCdpoaLO3sGlnE3QH_P8NFKGs130_provenance.
- NP14868.RAQYxkQt4w2sT-76EEOLPCdpoaLO3sGlnE3QH_P8NFKGs130_assertion SIO_000772 16531417 NP14868.RAQYxkQt4w2sT-76EEOLPCdpoaLO3sGlnE3QH_P8NFKGs130_provenance.
- NP14868.RAQYxkQt4w2sT-76EEOLPCdpoaLO3sGlnE3QH_P8NFKGs130_assertion evidence source_evidence_curated NP14868.RAQYxkQt4w2sT-76EEOLPCdpoaLO3sGlnE3QH_P8NFKGs130_provenance.
- NP14868.RAQYxkQt4w2sT-76EEOLPCdpoaLO3sGlnE3QH_P8NFKGs130_assertion description "[Hypoglycosylated alpha-DG indicated a lack of aggregation, and acetylcholine receptor (AChR) clustering was compromised in FCMD and the myodystrophy mouse, another model of secondary alpha-DGpathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP14868.RAQYxkQt4w2sT-76EEOLPCdpoaLO3sGlnE3QH_P8NFKGs130_provenance.