Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP27895.RAWvDj1oHH11yO6a-Yvh2iYTWyq7Qc1l9Ny6rggzT3eKY130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP27895.RAWvDj1oHH11yO6a-Yvh2iYTWyq7Qc1l9Ny6rggzT3eKY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP27895.RAWvDj1oHH11yO6a-Yvh2iYTWyq7Qc1l9Ny6rggzT3eKY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP27895.RAWvDj1oHH11yO6a-Yvh2iYTWyq7Qc1l9Ny6rggzT3eKY130_provenance.
- NP27895.RAWvDj1oHH11yO6a-Yvh2iYTWyq7Qc1l9Ny6rggzT3eKY130_assertion description "[Mutations of PTPN11, KRAS and SOS1 in the RAS-MAPK pathway cause approximately 60% of cases of Noonan syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP27895.RAWvDj1oHH11yO6a-Yvh2iYTWyq7Qc1l9Ny6rggzT3eKY130_provenance.
- NP27895.RAWvDj1oHH11yO6a-Yvh2iYTWyq7Qc1l9Ny6rggzT3eKY130_assertion evidence source_evidence_curated NP27895.RAWvDj1oHH11yO6a-Yvh2iYTWyq7Qc1l9Ny6rggzT3eKY130_provenance.
- NP27895.RAWvDj1oHH11yO6a-Yvh2iYTWyq7Qc1l9Ny6rggzT3eKY130_assertion SIO_000772 17603482 NP27895.RAWvDj1oHH11yO6a-Yvh2iYTWyq7Qc1l9Ny6rggzT3eKY130_provenance.
- NP27895.RAWvDj1oHH11yO6a-Yvh2iYTWyq7Qc1l9Ny6rggzT3eKY130_assertion wasDerivedFrom ctd_human-20150221 NP27895.RAWvDj1oHH11yO6a-Yvh2iYTWyq7Qc1l9Ny6rggzT3eKY130_provenance.
- NP27895.RAWvDj1oHH11yO6a-Yvh2iYTWyq7Qc1l9Ny6rggzT3eKY130_assertion wasGeneratedBy ECO_0000218 NP27895.RAWvDj1oHH11yO6a-Yvh2iYTWyq7Qc1l9Ny6rggzT3eKY130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP27895.RAWvDj1oHH11yO6a-Yvh2iYTWyq7Qc1l9Ny6rggzT3eKY130_provenance.