Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP647322.RA4c4h1KDc9sL0aGEaOnNFLak2VLWBqYldKxoCOl1G-vw130_assertion> ?p ?o ?g. }
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- NP647322.RA4c4h1KDc9sL0aGEaOnNFLak2VLWBqYldKxoCOl1G-vw130_assertion type Assertion NP647322.RA4c4h1KDc9sL0aGEaOnNFLak2VLWBqYldKxoCOl1G-vw130_head.
- NP647322.RA4c4h1KDc9sL0aGEaOnNFLak2VLWBqYldKxoCOl1G-vw130_assertion wasGeneratedBy ECO_0000203 NP647322.RA4c4h1KDc9sL0aGEaOnNFLak2VLWBqYldKxoCOl1G-vw130_provenance.
- NP647322.RA4c4h1KDc9sL0aGEaOnNFLak2VLWBqYldKxoCOl1G-vw130_assertion wasDerivedFrom befree-2016 NP647322.RA4c4h1KDc9sL0aGEaOnNFLak2VLWBqYldKxoCOl1G-vw130_provenance.
- NP647322.RA4c4h1KDc9sL0aGEaOnNFLak2VLWBqYldKxoCOl1G-vw130_assertion SIO_000772 18162506 NP647322.RA4c4h1KDc9sL0aGEaOnNFLak2VLWBqYldKxoCOl1G-vw130_provenance.
- NP647322.RA4c4h1KDc9sL0aGEaOnNFLak2VLWBqYldKxoCOl1G-vw130_assertion evidence source_evidence_literature NP647322.RA4c4h1KDc9sL0aGEaOnNFLak2VLWBqYldKxoCOl1G-vw130_provenance.
- NP647322.RA4c4h1KDc9sL0aGEaOnNFLak2VLWBqYldKxoCOl1G-vw130_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." NP647322.RA4c4h1KDc9sL0aGEaOnNFLak2VLWBqYldKxoCOl1G-vw130_provenance.