Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP376646.RA0PMaEXxpCUMDdWIgQ6eTVwYDJ6HuN8lUbdyodBMM5yA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP376646.RA0PMaEXxpCUMDdWIgQ6eTVwYDJ6HuN8lUbdyodBMM5yA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP376646.RA0PMaEXxpCUMDdWIgQ6eTVwYDJ6HuN8lUbdyodBMM5yA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP376646.RA0PMaEXxpCUMDdWIgQ6eTVwYDJ6HuN8lUbdyodBMM5yA130_provenance.
- NP376646.RA0PMaEXxpCUMDdWIgQ6eTVwYDJ6HuN8lUbdyodBMM5yA130_assertion description "[SHOC2 is mutated in Noonan syndrome and plays a key role in the activation of the ERK-MAPK pathway, which is upregulated in the majority of human cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP376646.RA0PMaEXxpCUMDdWIgQ6eTVwYDJ6HuN8lUbdyodBMM5yA130_provenance.
- NP376646.RA0PMaEXxpCUMDdWIgQ6eTVwYDJ6HuN8lUbdyodBMM5yA130_assertion evidence source_evidence_literature NP376646.RA0PMaEXxpCUMDdWIgQ6eTVwYDJ6HuN8lUbdyodBMM5yA130_provenance.
- NP376646.RA0PMaEXxpCUMDdWIgQ6eTVwYDJ6HuN8lUbdyodBMM5yA130_assertion SIO_000772 24211266 NP376646.RA0PMaEXxpCUMDdWIgQ6eTVwYDJ6HuN8lUbdyodBMM5yA130_provenance.
- NP376646.RA0PMaEXxpCUMDdWIgQ6eTVwYDJ6HuN8lUbdyodBMM5yA130_assertion wasDerivedFrom befree-20150227 NP376646.RA0PMaEXxpCUMDdWIgQ6eTVwYDJ6HuN8lUbdyodBMM5yA130_provenance.
- NP376646.RA0PMaEXxpCUMDdWIgQ6eTVwYDJ6HuN8lUbdyodBMM5yA130_assertion wasGeneratedBy ECO_0000203 NP376646.RA0PMaEXxpCUMDdWIgQ6eTVwYDJ6HuN8lUbdyodBMM5yA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP376646.RA0PMaEXxpCUMDdWIgQ6eTVwYDJ6HuN8lUbdyodBMM5yA130_provenance.