Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP790173.RAyNRNbN_UpgYoGJSNbgLqC7QUHlczcs6WTZoe0rykSvI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP790173.RAyNRNbN_UpgYoGJSNbgLqC7QUHlczcs6WTZoe0rykSvI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP790173.RAyNRNbN_UpgYoGJSNbgLqC7QUHlczcs6WTZoe0rykSvI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP790173.RAyNRNbN_UpgYoGJSNbgLqC7QUHlczcs6WTZoe0rykSvI130_provenance.
- NP790173.RAyNRNbN_UpgYoGJSNbgLqC7QUHlczcs6WTZoe0rykSvI130_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." NP790173.RAyNRNbN_UpgYoGJSNbgLqC7QUHlczcs6WTZoe0rykSvI130_provenance.
- NP790173.RAyNRNbN_UpgYoGJSNbgLqC7QUHlczcs6WTZoe0rykSvI130_assertion evidence source_evidence_literature NP790173.RAyNRNbN_UpgYoGJSNbgLqC7QUHlczcs6WTZoe0rykSvI130_provenance.
- NP790173.RAyNRNbN_UpgYoGJSNbgLqC7QUHlczcs6WTZoe0rykSvI130_assertion SIO_000772 11280716 NP790173.RAyNRNbN_UpgYoGJSNbgLqC7QUHlczcs6WTZoe0rykSvI130_provenance.
- NP790173.RAyNRNbN_UpgYoGJSNbgLqC7QUHlczcs6WTZoe0rykSvI130_assertion wasDerivedFrom befree-20140225 NP790173.RAyNRNbN_UpgYoGJSNbgLqC7QUHlczcs6WTZoe0rykSvI130_provenance.
- NP790173.RAyNRNbN_UpgYoGJSNbgLqC7QUHlczcs6WTZoe0rykSvI130_assertion wasGeneratedBy ECO_0000203 NP790173.RAyNRNbN_UpgYoGJSNbgLqC7QUHlczcs6WTZoe0rykSvI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP790173.RAyNRNbN_UpgYoGJSNbgLqC7QUHlczcs6WTZoe0rykSvI130_provenance.