Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_provenance.
- NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_assertion description "[We identified mutations in EXOSC3 in an additional 8 of 12 families with PCH1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_provenance.
- NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_assertion evidence source_evidence_curated NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_provenance.
- NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_assertion SIO_000772 22544365 NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_provenance.
- NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_assertion wasDerivedFrom ctd_human-20150221 NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_provenance.
- NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_assertion wasGeneratedBy ECO_0000218 NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP14098.RAV5YZWjftlUTe96TTnVeFecCBl-U4K-L8__SX3om9sF8130_provenance.