Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP217001.RAD30PZjU_0EqbSWBn8GjZr0jyapKhXDVuZdMistMSdzQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP217001.RAD30PZjU_0EqbSWBn8GjZr0jyapKhXDVuZdMistMSdzQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP217001.RAD30PZjU_0EqbSWBn8GjZr0jyapKhXDVuZdMistMSdzQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP217001.RAD30PZjU_0EqbSWBn8GjZr0jyapKhXDVuZdMistMSdzQ130_provenance.
- NP217001.RAD30PZjU_0EqbSWBn8GjZr0jyapKhXDVuZdMistMSdzQ130_assertion description "[The common somatic genetic changes in thyroid cancer of follicular cell origin (RET/PTC, NTRK, RAS, BRAF, PAX8-PPARgamma) are generally mutually exclusive, with distinct genotype-histologic subtype of thyroid cancer and genotype-phenotype associations observed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217001.RAD30PZjU_0EqbSWBn8GjZr0jyapKhXDVuZdMistMSdzQ130_provenance.
- NP217001.RAD30PZjU_0EqbSWBn8GjZr0jyapKhXDVuZdMistMSdzQ130_assertion evidence source_evidence_literature NP217001.RAD30PZjU_0EqbSWBn8GjZr0jyapKhXDVuZdMistMSdzQ130_provenance.
- NP217001.RAD30PZjU_0EqbSWBn8GjZr0jyapKhXDVuZdMistMSdzQ130_assertion SIO_000772 18043251 NP217001.RAD30PZjU_0EqbSWBn8GjZr0jyapKhXDVuZdMistMSdzQ130_provenance.
- NP217001.RAD30PZjU_0EqbSWBn8GjZr0jyapKhXDVuZdMistMSdzQ130_assertion wasDerivedFrom befree-20140225 NP217001.RAD30PZjU_0EqbSWBn8GjZr0jyapKhXDVuZdMistMSdzQ130_provenance.
- NP217001.RAD30PZjU_0EqbSWBn8GjZr0jyapKhXDVuZdMistMSdzQ130_assertion wasGeneratedBy ECO_0000203 NP217001.RAD30PZjU_0EqbSWBn8GjZr0jyapKhXDVuZdMistMSdzQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP217001.RAD30PZjU_0EqbSWBn8GjZr0jyapKhXDVuZdMistMSdzQ130_provenance.