Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP706764.RA3emfmBTfvyK1PGPmWnW6PwRWVm4pccDyr0mGy_151uk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP706764.RA3emfmBTfvyK1PGPmWnW6PwRWVm4pccDyr0mGy_151uk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP706764.RA3emfmBTfvyK1PGPmWnW6PwRWVm4pccDyr0mGy_151uk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP706764.RA3emfmBTfvyK1PGPmWnW6PwRWVm4pccDyr0mGy_151uk130_provenance.
- NP706764.RA3emfmBTfvyK1PGPmWnW6PwRWVm4pccDyr0mGy_151uk130_assertion description "[We assessed 71 children with JMML for NRAS, KRAS, and PTPN11 mutations and evaluated their clinical significance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP706764.RA3emfmBTfvyK1PGPmWnW6PwRWVm4pccDyr0mGy_151uk130_provenance.
- NP706764.RA3emfmBTfvyK1PGPmWnW6PwRWVm4pccDyr0mGy_151uk130_assertion evidence source_evidence_literature NP706764.RA3emfmBTfvyK1PGPmWnW6PwRWVm4pccDyr0mGy_151uk130_provenance.
- NP706764.RA3emfmBTfvyK1PGPmWnW6PwRWVm4pccDyr0mGy_151uk130_assertion SIO_000772 19047918 NP706764.RA3emfmBTfvyK1PGPmWnW6PwRWVm4pccDyr0mGy_151uk130_provenance.
- NP706764.RA3emfmBTfvyK1PGPmWnW6PwRWVm4pccDyr0mGy_151uk130_assertion wasDerivedFrom befree-2016 NP706764.RA3emfmBTfvyK1PGPmWnW6PwRWVm4pccDyr0mGy_151uk130_provenance.
- NP706764.RA3emfmBTfvyK1PGPmWnW6PwRWVm4pccDyr0mGy_151uk130_assertion wasGeneratedBy ECO_0000203 NP706764.RA3emfmBTfvyK1PGPmWnW6PwRWVm4pccDyr0mGy_151uk130_provenance.
- befree-2016 importedOn "2016-02-19" NP706764.RA3emfmBTfvyK1PGPmWnW6PwRWVm4pccDyr0mGy_151uk130_provenance.