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- source_evidence_literature type ECO_0000212 NP312709.RAe__4ANlS1Nb7izvnJ7L-KdBWEhnpvNuzC1a573UwFNM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP312709.RAe__4ANlS1Nb7izvnJ7L-KdBWEhnpvNuzC1a573UwFNM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP312709.RAe__4ANlS1Nb7izvnJ7L-KdBWEhnpvNuzC1a573UwFNM130_provenance.
- NP312709.RAe__4ANlS1Nb7izvnJ7L-KdBWEhnpvNuzC1a573UwFNM130_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." NP312709.RAe__4ANlS1Nb7izvnJ7L-KdBWEhnpvNuzC1a573UwFNM130_provenance.
- NP312709.RAe__4ANlS1Nb7izvnJ7L-KdBWEhnpvNuzC1a573UwFNM130_assertion evidence source_evidence_literature NP312709.RAe__4ANlS1Nb7izvnJ7L-KdBWEhnpvNuzC1a573UwFNM130_provenance.
- NP312709.RAe__4ANlS1Nb7izvnJ7L-KdBWEhnpvNuzC1a573UwFNM130_assertion SIO_000772 11280716 NP312709.RAe__4ANlS1Nb7izvnJ7L-KdBWEhnpvNuzC1a573UwFNM130_provenance.
- NP312709.RAe__4ANlS1Nb7izvnJ7L-KdBWEhnpvNuzC1a573UwFNM130_assertion wasDerivedFrom befree-2016 NP312709.RAe__4ANlS1Nb7izvnJ7L-KdBWEhnpvNuzC1a573UwFNM130_provenance.
- NP312709.RAe__4ANlS1Nb7izvnJ7L-KdBWEhnpvNuzC1a573UwFNM130_assertion wasGeneratedBy ECO_0000203 NP312709.RAe__4ANlS1Nb7izvnJ7L-KdBWEhnpvNuzC1a573UwFNM130_provenance.
- befree-2016 importedOn "2016-02-19" NP312709.RAe__4ANlS1Nb7izvnJ7L-KdBWEhnpvNuzC1a573UwFNM130_provenance.