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- NP306878.RAu2rpbF2idh_T83ujesUpn4Gc4wLHXdqK0xgRMlGwC1U130_assertion type Assertion NP306878.RAu2rpbF2idh_T83ujesUpn4Gc4wLHXdqK0xgRMlGwC1U130_head.
- NP306878.RAu2rpbF2idh_T83ujesUpn4Gc4wLHXdqK0xgRMlGwC1U130_assertion description "[CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP306878.RAu2rpbF2idh_T83ujesUpn4Gc4wLHXdqK0xgRMlGwC1U130_provenance.
- NP306878.RAu2rpbF2idh_T83ujesUpn4Gc4wLHXdqK0xgRMlGwC1U130_assertion evidence source_evidence_literature NP306878.RAu2rpbF2idh_T83ujesUpn4Gc4wLHXdqK0xgRMlGwC1U130_provenance.
- NP306878.RAu2rpbF2idh_T83ujesUpn4Gc4wLHXdqK0xgRMlGwC1U130_assertion SIO_000772 7640518 NP306878.RAu2rpbF2idh_T83ujesUpn4Gc4wLHXdqK0xgRMlGwC1U130_provenance.
- NP306878.RAu2rpbF2idh_T83ujesUpn4Gc4wLHXdqK0xgRMlGwC1U130_assertion wasDerivedFrom befree-20150227 NP306878.RAu2rpbF2idh_T83ujesUpn4Gc4wLHXdqK0xgRMlGwC1U130_provenance.
- NP306878.RAu2rpbF2idh_T83ujesUpn4Gc4wLHXdqK0xgRMlGwC1U130_assertion wasGeneratedBy ECO_0000203 NP306878.RAu2rpbF2idh_T83ujesUpn4Gc4wLHXdqK0xgRMlGwC1U130_provenance.