Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP5741.RADw5kHz1xeddeSfJNN1MSGnDMxtJiF7Sup-EQU9lF4BQ130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP5741.RADw5kHz1xeddeSfJNN1MSGnDMxtJiF7Sup-EQU9lF4BQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5741.RADw5kHz1xeddeSfJNN1MSGnDMxtJiF7Sup-EQU9lF4BQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5741.RADw5kHz1xeddeSfJNN1MSGnDMxtJiF7Sup-EQU9lF4BQ130_provenance.
- NP5741.RADw5kHz1xeddeSfJNN1MSGnDMxtJiF7Sup-EQU9lF4BQ130_assertion description "[In conclusion, our study suggests a pathogenic mechanism for MMIHS by identifying causative ACTG2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5741.RADw5kHz1xeddeSfJNN1MSGnDMxtJiF7Sup-EQU9lF4BQ130_provenance.
- NP5741.RADw5kHz1xeddeSfJNN1MSGnDMxtJiF7Sup-EQU9lF4BQ130_assertion evidence source_evidence_curated NP5741.RADw5kHz1xeddeSfJNN1MSGnDMxtJiF7Sup-EQU9lF4BQ130_provenance.
- NP5741.RADw5kHz1xeddeSfJNN1MSGnDMxtJiF7Sup-EQU9lF4BQ130_assertion SIO_000772 24337657 NP5741.RADw5kHz1xeddeSfJNN1MSGnDMxtJiF7Sup-EQU9lF4BQ130_provenance.
- NP5741.RADw5kHz1xeddeSfJNN1MSGnDMxtJiF7Sup-EQU9lF4BQ130_assertion wasDerivedFrom ctd_human-20150221 NP5741.RADw5kHz1xeddeSfJNN1MSGnDMxtJiF7Sup-EQU9lF4BQ130_provenance.
- NP5741.RADw5kHz1xeddeSfJNN1MSGnDMxtJiF7Sup-EQU9lF4BQ130_assertion wasGeneratedBy ECO_0000218 NP5741.RADw5kHz1xeddeSfJNN1MSGnDMxtJiF7Sup-EQU9lF4BQ130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP5741.RADw5kHz1xeddeSfJNN1MSGnDMxtJiF7Sup-EQU9lF4BQ130_provenance.