Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP484940.RA2qGTO29e22DSs7ug1QxqjCjX7o_IcpERi2P-dePTZZ8130_assertion> ?p ?o ?g. }
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- NP484940.RA2qGTO29e22DSs7ug1QxqjCjX7o_IcpERi2P-dePTZZ8130_assertion type Assertion NP484940.RA2qGTO29e22DSs7ug1QxqjCjX7o_IcpERi2P-dePTZZ8130_head.
- NP484940.RA2qGTO29e22DSs7ug1QxqjCjX7o_IcpERi2P-dePTZZ8130_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." NP484940.RA2qGTO29e22DSs7ug1QxqjCjX7o_IcpERi2P-dePTZZ8130_provenance.
- NP484940.RA2qGTO29e22DSs7ug1QxqjCjX7o_IcpERi2P-dePTZZ8130_assertion evidence source_evidence_literature NP484940.RA2qGTO29e22DSs7ug1QxqjCjX7o_IcpERi2P-dePTZZ8130_provenance.
- NP484940.RA2qGTO29e22DSs7ug1QxqjCjX7o_IcpERi2P-dePTZZ8130_assertion SIO_000772 14602786 NP484940.RA2qGTO29e22DSs7ug1QxqjCjX7o_IcpERi2P-dePTZZ8130_provenance.
- NP484940.RA2qGTO29e22DSs7ug1QxqjCjX7o_IcpERi2P-dePTZZ8130_assertion wasDerivedFrom befree-20140225 NP484940.RA2qGTO29e22DSs7ug1QxqjCjX7o_IcpERi2P-dePTZZ8130_provenance.
- NP484940.RA2qGTO29e22DSs7ug1QxqjCjX7o_IcpERi2P-dePTZZ8130_assertion wasGeneratedBy ECO_0000203 NP484940.RA2qGTO29e22DSs7ug1QxqjCjX7o_IcpERi2P-dePTZZ8130_provenance.