Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP136801.RA9zVI2ZVpj9K8TOGV-drp9jjX63E6jKiSINq6wELlij4130_assertion> ?p ?o ?g. }
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- NP136801.RA9zVI2ZVpj9K8TOGV-drp9jjX63E6jKiSINq6wELlij4130_assertion type Assertion NP136801.RA9zVI2ZVpj9K8TOGV-drp9jjX63E6jKiSINq6wELlij4130_head.
- NP136801.RA9zVI2ZVpj9K8TOGV-drp9jjX63E6jKiSINq6wELlij4130_assertion wasGeneratedBy ECO_0000203 NP136801.RA9zVI2ZVpj9K8TOGV-drp9jjX63E6jKiSINq6wELlij4130_provenance.
- NP136801.RA9zVI2ZVpj9K8TOGV-drp9jjX63E6jKiSINq6wELlij4130_assertion wasDerivedFrom gad-20150221 NP136801.RA9zVI2ZVpj9K8TOGV-drp9jjX63E6jKiSINq6wELlij4130_provenance.
- NP136801.RA9zVI2ZVpj9K8TOGV-drp9jjX63E6jKiSINq6wELlij4130_assertion SIO_000772 18162506 NP136801.RA9zVI2ZVpj9K8TOGV-drp9jjX63E6jKiSINq6wELlij4130_provenance.
- NP136801.RA9zVI2ZVpj9K8TOGV-drp9jjX63E6jKiSINq6wELlij4130_assertion evidence source_evidence_literature NP136801.RA9zVI2ZVpj9K8TOGV-drp9jjX63E6jKiSINq6wELlij4130_provenance.
- NP136801.RA9zVI2ZVpj9K8TOGV-drp9jjX63E6jKiSINq6wELlij4130_assertion description "[INS mutations are the second most common cause of PND and a rare cause of MODY.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136801.RA9zVI2ZVpj9K8TOGV-drp9jjX63E6jKiSINq6wELlij4130_provenance.