Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP25999.RALJphtUDl49ZeeLNnJppUTRpTZA6VAyuEetktavkda1Y130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP25999.RALJphtUDl49ZeeLNnJppUTRpTZA6VAyuEetktavkda1Y130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP25999.RALJphtUDl49ZeeLNnJppUTRpTZA6VAyuEetktavkda1Y130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP25999.RALJphtUDl49ZeeLNnJppUTRpTZA6VAyuEetktavkda1Y130_provenance.
- NP25999.RALJphtUDl49ZeeLNnJppUTRpTZA6VAyuEetktavkda1Y130_assertion description "[Refining the phenotype associated with MEF2C haploinsufficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP25999.RALJphtUDl49ZeeLNnJppUTRpTZA6VAyuEetktavkda1Y130_provenance.
- NP25999.RALJphtUDl49ZeeLNnJppUTRpTZA6VAyuEetktavkda1Y130_assertion evidence source_evidence_curated NP25999.RALJphtUDl49ZeeLNnJppUTRpTZA6VAyuEetktavkda1Y130_provenance.
- NP25999.RALJphtUDl49ZeeLNnJppUTRpTZA6VAyuEetktavkda1Y130_assertion SIO_000772 20412115 NP25999.RALJphtUDl49ZeeLNnJppUTRpTZA6VAyuEetktavkda1Y130_provenance.
- NP25999.RALJphtUDl49ZeeLNnJppUTRpTZA6VAyuEetktavkda1Y130_assertion wasDerivedFrom ctd_human-2016 NP25999.RALJphtUDl49ZeeLNnJppUTRpTZA6VAyuEetktavkda1Y130_provenance.
- NP25999.RALJphtUDl49ZeeLNnJppUTRpTZA6VAyuEetktavkda1Y130_assertion wasGeneratedBy ECO_0000218 NP25999.RALJphtUDl49ZeeLNnJppUTRpTZA6VAyuEetktavkda1Y130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP25999.RALJphtUDl49ZeeLNnJppUTRpTZA6VAyuEetktavkda1Y130_provenance.