Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_assertion> ?p ?o ?g. }
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- NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_assertion type Assertion NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_head.
- NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_assertion description "[This finding suggests that all families with a pedigree suggestive of FMTC should be regarded at risk from MEN 2A disease, at least when a critical mutation in the RET cysteine domain is detected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_provenance.
- NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_assertion evidence source_evidence_literature NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_provenance.
- NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_assertion SIO_000772 11280716 NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_provenance.
- NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_assertion wasDerivedFrom befree-20140225 NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_provenance.
- NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_assertion wasGeneratedBy ECO_0000203 NP218609.RAxcCWAmbK4wDDKFDmOPk4VeLMANHX9AdDhI4ZtanOpbg130_provenance.