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- NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_assertion type Assertion NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_head.
- NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_assertion description "[Although common RET mutations providing evidence of familial forms of MTC were identified in only 3 of 16 families, clinical and histologic features usually seen in inherited forms of MTC such as young age of occurrence, bilateral CCH or associated case in family were found in 11 of the remaining 14 patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_provenance.
- NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_assertion evidence source_evidence_literature NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_provenance.
- NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_assertion SIO_000772 15588381 NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_provenance.
- NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_assertion wasDerivedFrom befree-20140225 NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_provenance.
- NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_assertion wasGeneratedBy ECO_0000203 NP354272.RAOT-w4lB53fCwViUG7640XJRdEPqPyk761cos6vCh--c130_provenance.