Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP493868.RADs4HdcVASCbJ5bwHB5CDAcflLWbuL-VoE9jo5reElVg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP493868.RADs4HdcVASCbJ5bwHB5CDAcflLWbuL-VoE9jo5reElVg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP493868.RADs4HdcVASCbJ5bwHB5CDAcflLWbuL-VoE9jo5reElVg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP493868.RADs4HdcVASCbJ5bwHB5CDAcflLWbuL-VoE9jo5reElVg130_provenance.
- NP493868.RADs4HdcVASCbJ5bwHB5CDAcflLWbuL-VoE9jo5reElVg130_assertion description "[A meta-review of the literature on familial PTC (FPTC) was undertaken, and characteristics of families with frequent occurrence of PTC or MNG (or both) were summarized.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493868.RADs4HdcVASCbJ5bwHB5CDAcflLWbuL-VoE9jo5reElVg130_provenance.
- NP493868.RADs4HdcVASCbJ5bwHB5CDAcflLWbuL-VoE9jo5reElVg130_assertion evidence source_evidence_literature NP493868.RADs4HdcVASCbJ5bwHB5CDAcflLWbuL-VoE9jo5reElVg130_provenance.
- NP493868.RADs4HdcVASCbJ5bwHB5CDAcflLWbuL-VoE9jo5reElVg130_assertion SIO_000772 11038215 NP493868.RADs4HdcVASCbJ5bwHB5CDAcflLWbuL-VoE9jo5reElVg130_provenance.
- NP493868.RADs4HdcVASCbJ5bwHB5CDAcflLWbuL-VoE9jo5reElVg130_assertion wasDerivedFrom befree-20140225 NP493868.RADs4HdcVASCbJ5bwHB5CDAcflLWbuL-VoE9jo5reElVg130_provenance.
- NP493868.RADs4HdcVASCbJ5bwHB5CDAcflLWbuL-VoE9jo5reElVg130_assertion wasGeneratedBy ECO_0000203 NP493868.RADs4HdcVASCbJ5bwHB5CDAcflLWbuL-VoE9jo5reElVg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP493868.RADs4HdcVASCbJ5bwHB5CDAcflLWbuL-VoE9jo5reElVg130_provenance.