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- source_evidence_literature type ECO_0000212 NP599814.RA-dFypuH5c0PG6tkaCoU_wuleEBDsLqlLyQltxLM3Ei0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP599814.RA-dFypuH5c0PG6tkaCoU_wuleEBDsLqlLyQltxLM3Ei0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP599814.RA-dFypuH5c0PG6tkaCoU_wuleEBDsLqlLyQltxLM3Ei0130_provenance.
- NP599814.RA-dFypuH5c0PG6tkaCoU_wuleEBDsLqlLyQltxLM3Ei0130_assertion description "[A large family with hereditary MTC: role of RET genetic analysis in differential diagnosis between MEN 2A and FMTC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP599814.RA-dFypuH5c0PG6tkaCoU_wuleEBDsLqlLyQltxLM3Ei0130_provenance.
- NP599814.RA-dFypuH5c0PG6tkaCoU_wuleEBDsLqlLyQltxLM3Ei0130_assertion evidence source_evidence_literature NP599814.RA-dFypuH5c0PG6tkaCoU_wuleEBDsLqlLyQltxLM3Ei0130_provenance.
- NP599814.RA-dFypuH5c0PG6tkaCoU_wuleEBDsLqlLyQltxLM3Ei0130_assertion SIO_000772 11280716 NP599814.RA-dFypuH5c0PG6tkaCoU_wuleEBDsLqlLyQltxLM3Ei0130_provenance.
- NP599814.RA-dFypuH5c0PG6tkaCoU_wuleEBDsLqlLyQltxLM3Ei0130_assertion wasDerivedFrom befree-20150227 NP599814.RA-dFypuH5c0PG6tkaCoU_wuleEBDsLqlLyQltxLM3Ei0130_provenance.
- NP599814.RA-dFypuH5c0PG6tkaCoU_wuleEBDsLqlLyQltxLM3Ei0130_assertion wasGeneratedBy ECO_0000203 NP599814.RA-dFypuH5c0PG6tkaCoU_wuleEBDsLqlLyQltxLM3Ei0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP599814.RA-dFypuH5c0PG6tkaCoU_wuleEBDsLqlLyQltxLM3Ei0130_provenance.