Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP28120.RAEOOoc7B9kiBp9n5fGPk3jbtJ6dzBB5y-eLgOG_cFIIY130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP28120.RAEOOoc7B9kiBp9n5fGPk3jbtJ6dzBB5y-eLgOG_cFIIY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP28120.RAEOOoc7B9kiBp9n5fGPk3jbtJ6dzBB5y-eLgOG_cFIIY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP28120.RAEOOoc7B9kiBp9n5fGPk3jbtJ6dzBB5y-eLgOG_cFIIY130_provenance.
- NP28120.RAEOOoc7B9kiBp9n5fGPk3jbtJ6dzBB5y-eLgOG_cFIIY130_assertion description "[Germline gain-of-function mutations in RAF1 cause Noonan syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP28120.RAEOOoc7B9kiBp9n5fGPk3jbtJ6dzBB5y-eLgOG_cFIIY130_provenance.
- NP28120.RAEOOoc7B9kiBp9n5fGPk3jbtJ6dzBB5y-eLgOG_cFIIY130_assertion evidence source_evidence_curated NP28120.RAEOOoc7B9kiBp9n5fGPk3jbtJ6dzBB5y-eLgOG_cFIIY130_provenance.
- NP28120.RAEOOoc7B9kiBp9n5fGPk3jbtJ6dzBB5y-eLgOG_cFIIY130_assertion SIO_000772 17603482 NP28120.RAEOOoc7B9kiBp9n5fGPk3jbtJ6dzBB5y-eLgOG_cFIIY130_provenance.
- NP28120.RAEOOoc7B9kiBp9n5fGPk3jbtJ6dzBB5y-eLgOG_cFIIY130_assertion wasDerivedFrom ctd_human-20150221 NP28120.RAEOOoc7B9kiBp9n5fGPk3jbtJ6dzBB5y-eLgOG_cFIIY130_provenance.
- NP28120.RAEOOoc7B9kiBp9n5fGPk3jbtJ6dzBB5y-eLgOG_cFIIY130_assertion wasGeneratedBy ECO_0000218 NP28120.RAEOOoc7B9kiBp9n5fGPk3jbtJ6dzBB5y-eLgOG_cFIIY130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP28120.RAEOOoc7B9kiBp9n5fGPk3jbtJ6dzBB5y-eLgOG_cFIIY130_provenance.