Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP5217.RAUGmPPhKnGogVns3mG8Z2BLATeBpLcgWLG_z6qBscP-k130_assertion> ?p ?o ?g. }
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- NP5217.RAUGmPPhKnGogVns3mG8Z2BLATeBpLcgWLG_z6qBscP-k130_assertion type Assertion NP5217.RAUGmPPhKnGogVns3mG8Z2BLATeBpLcgWLG_z6qBscP-k130_head.
- NP5217.RAUGmPPhKnGogVns3mG8Z2BLATeBpLcgWLG_z6qBscP-k130_assertion wasGeneratedBy ECO_0000218 NP5217.RAUGmPPhKnGogVns3mG8Z2BLATeBpLcgWLG_z6qBscP-k130_provenance.
- NP5217.RAUGmPPhKnGogVns3mG8Z2BLATeBpLcgWLG_z6qBscP-k130_assertion wasDerivedFrom uniprot-2016 NP5217.RAUGmPPhKnGogVns3mG8Z2BLATeBpLcgWLG_z6qBscP-k130_provenance.
- NP5217.RAUGmPPhKnGogVns3mG8Z2BLATeBpLcgWLG_z6qBscP-k130_assertion SIO_000772 18162506 NP5217.RAUGmPPhKnGogVns3mG8Z2BLATeBpLcgWLG_z6qBscP-k130_provenance.
- NP5217.RAUGmPPhKnGogVns3mG8Z2BLATeBpLcgWLG_z6qBscP-k130_assertion evidence source_evidence_curated NP5217.RAUGmPPhKnGogVns3mG8Z2BLATeBpLcgWLG_z6qBscP-k130_provenance.
- NP5217.RAUGmPPhKnGogVns3mG8Z2BLATeBpLcgWLG_z6qBscP-k130_assertion description "[Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5217.RAUGmPPhKnGogVns3mG8Z2BLATeBpLcgWLG_z6qBscP-k130_provenance.