Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP799549.RAmmAgxGYQAiQrZUsQ3kQDSBdD91CN_HVsznfWEajws9k130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP799549.RAmmAgxGYQAiQrZUsQ3kQDSBdD91CN_HVsznfWEajws9k130_assertion type Assertion NP799549.RAmmAgxGYQAiQrZUsQ3kQDSBdD91CN_HVsznfWEajws9k130_head.
- NP799549.RAmmAgxGYQAiQrZUsQ3kQDSBdD91CN_HVsznfWEajws9k130_assertion wasGeneratedBy ECO_0000203 NP799549.RAmmAgxGYQAiQrZUsQ3kQDSBdD91CN_HVsznfWEajws9k130_provenance.
- NP799549.RAmmAgxGYQAiQrZUsQ3kQDSBdD91CN_HVsznfWEajws9k130_assertion wasDerivedFrom befree-2016 NP799549.RAmmAgxGYQAiQrZUsQ3kQDSBdD91CN_HVsznfWEajws9k130_provenance.
- NP799549.RAmmAgxGYQAiQrZUsQ3kQDSBdD91CN_HVsznfWEajws9k130_assertion SIO_000772 20226046 NP799549.RAmmAgxGYQAiQrZUsQ3kQDSBdD91CN_HVsznfWEajws9k130_provenance.
- NP799549.RAmmAgxGYQAiQrZUsQ3kQDSBdD91CN_HVsznfWEajws9k130_assertion evidence source_evidence_literature NP799549.RAmmAgxGYQAiQrZUsQ3kQDSBdD91CN_HVsznfWEajws9k130_provenance.
- NP799549.RAmmAgxGYQAiQrZUsQ3kQDSBdD91CN_HVsznfWEajws9k130_assertion description "[Insulin gene (INS) mutations have recently been described as a common cause of permanent neonatal diabetes (PNDM) and a rare cause of diabetes diagnosed in childhood or adulthood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799549.RAmmAgxGYQAiQrZUsQ3kQDSBdD91CN_HVsznfWEajws9k130_provenance.