Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP419512.RAAr_MGuLstomnzdRD-U_GxGotNx1Tu8aXnC7gpSoRHjo130_assertion> ?p ?o ?g. }
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- NP419512.RAAr_MGuLstomnzdRD-U_GxGotNx1Tu8aXnC7gpSoRHjo130_assertion type Assertion NP419512.RAAr_MGuLstomnzdRD-U_GxGotNx1Tu8aXnC7gpSoRHjo130_head.
- NP419512.RAAr_MGuLstomnzdRD-U_GxGotNx1Tu8aXnC7gpSoRHjo130_assertion description "[It is likely that the mutation causes familial medullary thyroid carcinoma (FMTC), because no other mutation was found in RET, the mutation cosegregates with medullary thyroid carcinoma (MTC) or C cell hyperplasia (CCH) in patients subjected to surgery, and family members without the mutation are clinically unaffected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419512.RAAr_MGuLstomnzdRD-U_GxGotNx1Tu8aXnC7gpSoRHjo130_provenance.
- NP419512.RAAr_MGuLstomnzdRD-U_GxGotNx1Tu8aXnC7gpSoRHjo130_assertion evidence source_evidence_literature NP419512.RAAr_MGuLstomnzdRD-U_GxGotNx1Tu8aXnC7gpSoRHjo130_provenance.
- NP419512.RAAr_MGuLstomnzdRD-U_GxGotNx1Tu8aXnC7gpSoRHjo130_assertion SIO_000772 14602786 NP419512.RAAr_MGuLstomnzdRD-U_GxGotNx1Tu8aXnC7gpSoRHjo130_provenance.
- NP419512.RAAr_MGuLstomnzdRD-U_GxGotNx1Tu8aXnC7gpSoRHjo130_assertion wasDerivedFrom befree-2016 NP419512.RAAr_MGuLstomnzdRD-U_GxGotNx1Tu8aXnC7gpSoRHjo130_provenance.
- NP419512.RAAr_MGuLstomnzdRD-U_GxGotNx1Tu8aXnC7gpSoRHjo130_assertion wasGeneratedBy ECO_0000203 NP419512.RAAr_MGuLstomnzdRD-U_GxGotNx1Tu8aXnC7gpSoRHjo130_provenance.