Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP256812.RAf725Pge_dB_sGKGRWO5__TFKYSlwmOawv034iBdOlzE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP256812.RAf725Pge_dB_sGKGRWO5__TFKYSlwmOawv034iBdOlzE130_assertion type Assertion NP256812.RAf725Pge_dB_sGKGRWO5__TFKYSlwmOawv034iBdOlzE130_head.
- NP256812.RAf725Pge_dB_sGKGRWO5__TFKYSlwmOawv034iBdOlzE130_assertion wasGeneratedBy ECO_0000203 NP256812.RAf725Pge_dB_sGKGRWO5__TFKYSlwmOawv034iBdOlzE130_provenance.
- NP256812.RAf725Pge_dB_sGKGRWO5__TFKYSlwmOawv034iBdOlzE130_assertion wasDerivedFrom befree-2016 NP256812.RAf725Pge_dB_sGKGRWO5__TFKYSlwmOawv034iBdOlzE130_provenance.
- NP256812.RAf725Pge_dB_sGKGRWO5__TFKYSlwmOawv034iBdOlzE130_assertion SIO_000772 10396361 NP256812.RAf725Pge_dB_sGKGRWO5__TFKYSlwmOawv034iBdOlzE130_provenance.
- NP256812.RAf725Pge_dB_sGKGRWO5__TFKYSlwmOawv034iBdOlzE130_assertion evidence source_evidence_literature NP256812.RAf725Pge_dB_sGKGRWO5__TFKYSlwmOawv034iBdOlzE130_provenance.
- NP256812.RAf725Pge_dB_sGKGRWO5__TFKYSlwmOawv034iBdOlzE130_assertion description "[Familial hyperparathyroidism may occur as familial isolated hyperparathyroidism (FIHP) or as part of an inherited syndrome, in particular multiple endocrine neoplasia types 1 and 2A (MEN1, MEN2A) and hyperparathyroidism-jaw tumour (HPT-JT) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256812.RAf725Pge_dB_sGKGRWO5__TFKYSlwmOawv034iBdOlzE130_provenance.