Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_provenance.
- NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_assertion description "[Initially a codon 634 (exon 11) mutation was found in approximately 85% of patients with MEN 2A, and germline mutations in FMTC kindreds were more equally distributed throughout the RET proto-onocogene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_provenance.
- NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_assertion evidence source_evidence_literature NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_provenance.
- NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_assertion SIO_000772 17605401 NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_provenance.
- NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_assertion wasDerivedFrom befree-2016 NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_provenance.
- NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_assertion wasGeneratedBy ECO_0000203 NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_provenance.
- befree-2016 importedOn "2016-02-19" NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_provenance.