Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP474870.RAkURlKtJhSc_eBjS_g614RS7rlX8btuqAuU6FrEGSK90130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP474870.RAkURlKtJhSc_eBjS_g614RS7rlX8btuqAuU6FrEGSK90130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP474870.RAkURlKtJhSc_eBjS_g614RS7rlX8btuqAuU6FrEGSK90130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP474870.RAkURlKtJhSc_eBjS_g614RS7rlX8btuqAuU6FrEGSK90130_provenance.
- NP474870.RAkURlKtJhSc_eBjS_g614RS7rlX8btuqAuU6FrEGSK90130_assertion description "[Direct sequencing analysis showed that all mutations were CAA (Gln) to CGA (Arg) transition of codon 61, except for CAA to AAA transversion in one case of follicular carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP474870.RAkURlKtJhSc_eBjS_g614RS7rlX8btuqAuU6FrEGSK90130_provenance.
- NP474870.RAkURlKtJhSc_eBjS_g614RS7rlX8btuqAuU6FrEGSK90130_assertion evidence source_evidence_literature NP474870.RAkURlKtJhSc_eBjS_g614RS7rlX8btuqAuU6FrEGSK90130_provenance.
- NP474870.RAkURlKtJhSc_eBjS_g614RS7rlX8btuqAuU6FrEGSK90130_assertion SIO_000772 7704243 NP474870.RAkURlKtJhSc_eBjS_g614RS7rlX8btuqAuU6FrEGSK90130_provenance.
- NP474870.RAkURlKtJhSc_eBjS_g614RS7rlX8btuqAuU6FrEGSK90130_assertion wasDerivedFrom befree-20140225 NP474870.RAkURlKtJhSc_eBjS_g614RS7rlX8btuqAuU6FrEGSK90130_provenance.
- NP474870.RAkURlKtJhSc_eBjS_g614RS7rlX8btuqAuU6FrEGSK90130_assertion wasGeneratedBy ECO_0000203 NP474870.RAkURlKtJhSc_eBjS_g614RS7rlX8btuqAuU6FrEGSK90130_provenance.
- befree-20140225 importedOn "2014-02-25" NP474870.RAkURlKtJhSc_eBjS_g614RS7rlX8btuqAuU6FrEGSK90130_provenance.