Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP372078.RA7mwuUTtU7wf4C_ndy8N5--srrb3MkXlVAbktHOkOLAY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP372078.RA7mwuUTtU7wf4C_ndy8N5--srrb3MkXlVAbktHOkOLAY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP372078.RA7mwuUTtU7wf4C_ndy8N5--srrb3MkXlVAbktHOkOLAY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP372078.RA7mwuUTtU7wf4C_ndy8N5--srrb3MkXlVAbktHOkOLAY130_provenance.
- NP372078.RA7mwuUTtU7wf4C_ndy8N5--srrb3MkXlVAbktHOkOLAY130_assertion description "[RSK2 mutations in CLS patients are extremely heterogeneous.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372078.RA7mwuUTtU7wf4C_ndy8N5--srrb3MkXlVAbktHOkOLAY130_provenance.
- NP372078.RA7mwuUTtU7wf4C_ndy8N5--srrb3MkXlVAbktHOkOLAY130_assertion evidence source_evidence_literature NP372078.RA7mwuUTtU7wf4C_ndy8N5--srrb3MkXlVAbktHOkOLAY130_provenance.
- NP372078.RA7mwuUTtU7wf4C_ndy8N5--srrb3MkXlVAbktHOkOLAY130_assertion SIO_000772 12393804 NP372078.RA7mwuUTtU7wf4C_ndy8N5--srrb3MkXlVAbktHOkOLAY130_provenance.
- NP372078.RA7mwuUTtU7wf4C_ndy8N5--srrb3MkXlVAbktHOkOLAY130_assertion wasDerivedFrom befree-2016 NP372078.RA7mwuUTtU7wf4C_ndy8N5--srrb3MkXlVAbktHOkOLAY130_provenance.
- NP372078.RA7mwuUTtU7wf4C_ndy8N5--srrb3MkXlVAbktHOkOLAY130_assertion wasGeneratedBy ECO_0000203 NP372078.RA7mwuUTtU7wf4C_ndy8N5--srrb3MkXlVAbktHOkOLAY130_provenance.
- befree-2016 importedOn "2016-02-19" NP372078.RA7mwuUTtU7wf4C_ndy8N5--srrb3MkXlVAbktHOkOLAY130_provenance.