Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP5626.RAEGx-me_T4qpFapz_l9LE1AiiRT7fkzAHortoOjJu2l8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP5626.RAEGx-me_T4qpFapz_l9LE1AiiRT7fkzAHortoOjJu2l8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5626.RAEGx-me_T4qpFapz_l9LE1AiiRT7fkzAHortoOjJu2l8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5626.RAEGx-me_T4qpFapz_l9LE1AiiRT7fkzAHortoOjJu2l8130_provenance.
- NP5626.RAEGx-me_T4qpFapz_l9LE1AiiRT7fkzAHortoOjJu2l8130_assertion description "[No obvious correlation was observed between the position or type of the RSK2 mutations and the severity or particular clinical features of CLS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5626.RAEGx-me_T4qpFapz_l9LE1AiiRT7fkzAHortoOjJu2l8130_provenance.
- NP5626.RAEGx-me_T4qpFapz_l9LE1AiiRT7fkzAHortoOjJu2l8130_assertion evidence source_evidence_curated NP5626.RAEGx-me_T4qpFapz_l9LE1AiiRT7fkzAHortoOjJu2l8130_provenance.
- NP5626.RAEGx-me_T4qpFapz_l9LE1AiiRT7fkzAHortoOjJu2l8130_assertion SIO_000772 9837815 NP5626.RAEGx-me_T4qpFapz_l9LE1AiiRT7fkzAHortoOjJu2l8130_provenance.
- NP5626.RAEGx-me_T4qpFapz_l9LE1AiiRT7fkzAHortoOjJu2l8130_assertion wasDerivedFrom uniprot-20130724 NP5626.RAEGx-me_T4qpFapz_l9LE1AiiRT7fkzAHortoOjJu2l8130_provenance.
- NP5626.RAEGx-me_T4qpFapz_l9LE1AiiRT7fkzAHortoOjJu2l8130_assertion wasGeneratedBy ECO_0000218 NP5626.RAEGx-me_T4qpFapz_l9LE1AiiRT7fkzAHortoOjJu2l8130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP5626.RAEGx-me_T4qpFapz_l9LE1AiiRT7fkzAHortoOjJu2l8130_provenance.