Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP21495.RArSkvTQqEVIa_KzKc0mpaRiAxFo-MZdfeZf09gcRyzkg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP21495.RArSkvTQqEVIa_KzKc0mpaRiAxFo-MZdfeZf09gcRyzkg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP21495.RArSkvTQqEVIa_KzKc0mpaRiAxFo-MZdfeZf09gcRyzkg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP21495.RArSkvTQqEVIa_KzKc0mpaRiAxFo-MZdfeZf09gcRyzkg130_provenance.
- NP21495.RArSkvTQqEVIa_KzKc0mpaRiAxFo-MZdfeZf09gcRyzkg130_assertion description "[The position of the mutations and the loss of heterozygosity of MAP3K5 and MAP3K9 in 85% and 67% of melanoma samples, respectively, together suggest that the mutations are likely to be inactivating.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP21495.RArSkvTQqEVIa_KzKc0mpaRiAxFo-MZdfeZf09gcRyzkg130_provenance.
- NP21495.RArSkvTQqEVIa_KzKc0mpaRiAxFo-MZdfeZf09gcRyzkg130_assertion evidence source_evidence_curated NP21495.RArSkvTQqEVIa_KzKc0mpaRiAxFo-MZdfeZf09gcRyzkg130_provenance.
- NP21495.RArSkvTQqEVIa_KzKc0mpaRiAxFo-MZdfeZf09gcRyzkg130_assertion SIO_000772 22197930 NP21495.RArSkvTQqEVIa_KzKc0mpaRiAxFo-MZdfeZf09gcRyzkg130_provenance.
- NP21495.RArSkvTQqEVIa_KzKc0mpaRiAxFo-MZdfeZf09gcRyzkg130_assertion wasDerivedFrom ctd_human-20150221 NP21495.RArSkvTQqEVIa_KzKc0mpaRiAxFo-MZdfeZf09gcRyzkg130_provenance.
- NP21495.RArSkvTQqEVIa_KzKc0mpaRiAxFo-MZdfeZf09gcRyzkg130_assertion wasGeneratedBy ECO_0000218 NP21495.RArSkvTQqEVIa_KzKc0mpaRiAxFo-MZdfeZf09gcRyzkg130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP21495.RArSkvTQqEVIa_KzKc0mpaRiAxFo-MZdfeZf09gcRyzkg130_provenance.