Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP30507.RAqXefMcDH8n2LVacsk98cPQtEzjCkJm0rJ_mUrpsf4ig130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP30507.RAqXefMcDH8n2LVacsk98cPQtEzjCkJm0rJ_mUrpsf4ig130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP30507.RAqXefMcDH8n2LVacsk98cPQtEzjCkJm0rJ_mUrpsf4ig130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP30507.RAqXefMcDH8n2LVacsk98cPQtEzjCkJm0rJ_mUrpsf4ig130_provenance.
- NP30507.RAqXefMcDH8n2LVacsk98cPQtEzjCkJm0rJ_mUrpsf4ig130_assertion description "[Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30507.RAqXefMcDH8n2LVacsk98cPQtEzjCkJm0rJ_mUrpsf4ig130_provenance.
- NP30507.RAqXefMcDH8n2LVacsk98cPQtEzjCkJm0rJ_mUrpsf4ig130_assertion evidence source_evidence_curated NP30507.RAqXefMcDH8n2LVacsk98cPQtEzjCkJm0rJ_mUrpsf4ig130_provenance.
- NP30507.RAqXefMcDH8n2LVacsk98cPQtEzjCkJm0rJ_mUrpsf4ig130_assertion SIO_000772 22158539 NP30507.RAqXefMcDH8n2LVacsk98cPQtEzjCkJm0rJ_mUrpsf4ig130_provenance.
- NP30507.RAqXefMcDH8n2LVacsk98cPQtEzjCkJm0rJ_mUrpsf4ig130_assertion wasDerivedFrom ctd_human-2016 NP30507.RAqXefMcDH8n2LVacsk98cPQtEzjCkJm0rJ_mUrpsf4ig130_provenance.
- NP30507.RAqXefMcDH8n2LVacsk98cPQtEzjCkJm0rJ_mUrpsf4ig130_assertion wasGeneratedBy ECO_0000218 NP30507.RAqXefMcDH8n2LVacsk98cPQtEzjCkJm0rJ_mUrpsf4ig130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP30507.RAqXefMcDH8n2LVacsk98cPQtEzjCkJm0rJ_mUrpsf4ig130_provenance.