Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP21177.RAd8B0403_9hcS-wN-i9Nr-FlKbIUrGJ8QIb_Ch2OJn2w130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP21177.RAd8B0403_9hcS-wN-i9Nr-FlKbIUrGJ8QIb_Ch2OJn2w130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP21177.RAd8B0403_9hcS-wN-i9Nr-FlKbIUrGJ8QIb_Ch2OJn2w130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP21177.RAd8B0403_9hcS-wN-i9Nr-FlKbIUrGJ8QIb_Ch2OJn2w130_provenance.
- NP21177.RAd8B0403_9hcS-wN-i9Nr-FlKbIUrGJ8QIb_Ch2OJn2w130_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." NP21177.RAd8B0403_9hcS-wN-i9Nr-FlKbIUrGJ8QIb_Ch2OJn2w130_provenance.
- NP21177.RAd8B0403_9hcS-wN-i9Nr-FlKbIUrGJ8QIb_Ch2OJn2w130_assertion evidence source_evidence_curated NP21177.RAd8B0403_9hcS-wN-i9Nr-FlKbIUrGJ8QIb_Ch2OJn2w130_provenance.
- NP21177.RAd8B0403_9hcS-wN-i9Nr-FlKbIUrGJ8QIb_Ch2OJn2w130_assertion SIO_000772 17603483 NP21177.RAd8B0403_9hcS-wN-i9Nr-FlKbIUrGJ8QIb_Ch2OJn2w130_provenance.
- NP21177.RAd8B0403_9hcS-wN-i9Nr-FlKbIUrGJ8QIb_Ch2OJn2w130_assertion wasDerivedFrom ctd_human-20130708 NP21177.RAd8B0403_9hcS-wN-i9Nr-FlKbIUrGJ8QIb_Ch2OJn2w130_provenance.
- NP21177.RAd8B0403_9hcS-wN-i9Nr-FlKbIUrGJ8QIb_Ch2OJn2w130_assertion wasGeneratedBy ECO_0000218 NP21177.RAd8B0403_9hcS-wN-i9Nr-FlKbIUrGJ8QIb_Ch2OJn2w130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP21177.RAd8B0403_9hcS-wN-i9Nr-FlKbIUrGJ8QIb_Ch2OJn2w130_provenance.