Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP30925.RAcGzGiZwVrs8-kHzsCdlr0_-52ovfw13-9tMWmIs0Oqc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP30925.RAcGzGiZwVrs8-kHzsCdlr0_-52ovfw13-9tMWmIs0Oqc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP30925.RAcGzGiZwVrs8-kHzsCdlr0_-52ovfw13-9tMWmIs0Oqc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP30925.RAcGzGiZwVrs8-kHzsCdlr0_-52ovfw13-9tMWmIs0Oqc130_provenance.
- NP30925.RAcGzGiZwVrs8-kHzsCdlr0_-52ovfw13-9tMWmIs0Oqc130_assertion description "[Increased RAS signaling owing to PTPN11, SOS1 and KRAS mutations causes approximately 60% of Noonan syndrome cases, and PTPN11 mutations cause 90% of LEOPARD syndrome cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30925.RAcGzGiZwVrs8-kHzsCdlr0_-52ovfw13-9tMWmIs0Oqc130_provenance.
- NP30925.RAcGzGiZwVrs8-kHzsCdlr0_-52ovfw13-9tMWmIs0Oqc130_assertion evidence source_evidence_curated NP30925.RAcGzGiZwVrs8-kHzsCdlr0_-52ovfw13-9tMWmIs0Oqc130_provenance.
- NP30925.RAcGzGiZwVrs8-kHzsCdlr0_-52ovfw13-9tMWmIs0Oqc130_assertion SIO_000772 17603483 NP30925.RAcGzGiZwVrs8-kHzsCdlr0_-52ovfw13-9tMWmIs0Oqc130_provenance.
- NP30925.RAcGzGiZwVrs8-kHzsCdlr0_-52ovfw13-9tMWmIs0Oqc130_assertion wasDerivedFrom ctd_human-20150221 NP30925.RAcGzGiZwVrs8-kHzsCdlr0_-52ovfw13-9tMWmIs0Oqc130_provenance.
- NP30925.RAcGzGiZwVrs8-kHzsCdlr0_-52ovfw13-9tMWmIs0Oqc130_assertion wasGeneratedBy ECO_0000218 NP30925.RAcGzGiZwVrs8-kHzsCdlr0_-52ovfw13-9tMWmIs0Oqc130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP30925.RAcGzGiZwVrs8-kHzsCdlr0_-52ovfw13-9tMWmIs0Oqc130_provenance.