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- source_evidence_literature type ECO_0000212 NP312703.RA5TPe6H4YgHOVA_5MXdYT13f0uJlhj6AgQebaaAVbSg8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP312703.RA5TPe6H4YgHOVA_5MXdYT13f0uJlhj6AgQebaaAVbSg8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP312703.RA5TPe6H4YgHOVA_5MXdYT13f0uJlhj6AgQebaaAVbSg8130_provenance.
- NP312703.RA5TPe6H4YgHOVA_5MXdYT13f0uJlhj6AgQebaaAVbSg8130_assertion description "[However, the strong association of RET mutation at codon 634 with the presence of pheochromocytoma in MEN 2 disease suggested a more rigorous management in all gene carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312703.RA5TPe6H4YgHOVA_5MXdYT13f0uJlhj6AgQebaaAVbSg8130_provenance.
- NP312703.RA5TPe6H4YgHOVA_5MXdYT13f0uJlhj6AgQebaaAVbSg8130_assertion evidence source_evidence_literature NP312703.RA5TPe6H4YgHOVA_5MXdYT13f0uJlhj6AgQebaaAVbSg8130_provenance.
- NP312703.RA5TPe6H4YgHOVA_5MXdYT13f0uJlhj6AgQebaaAVbSg8130_assertion SIO_000772 11280716 NP312703.RA5TPe6H4YgHOVA_5MXdYT13f0uJlhj6AgQebaaAVbSg8130_provenance.
- NP312703.RA5TPe6H4YgHOVA_5MXdYT13f0uJlhj6AgQebaaAVbSg8130_assertion wasDerivedFrom befree-2016 NP312703.RA5TPe6H4YgHOVA_5MXdYT13f0uJlhj6AgQebaaAVbSg8130_provenance.
- NP312703.RA5TPe6H4YgHOVA_5MXdYT13f0uJlhj6AgQebaaAVbSg8130_assertion wasGeneratedBy ECO_0000203 NP312703.RA5TPe6H4YgHOVA_5MXdYT13f0uJlhj6AgQebaaAVbSg8130_provenance.
- befree-2016 importedOn "2016-02-19" NP312703.RA5TPe6H4YgHOVA_5MXdYT13f0uJlhj6AgQebaaAVbSg8130_provenance.