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- NP19503.RA-5LoLQFgfLMZk3NeIhRRxYx3_6pyyn65_h0UlKvNPww130_assertion type Assertion NP19503.RA-5LoLQFgfLMZk3NeIhRRxYx3_6pyyn65_h0UlKvNPww130_head.
- NP19503.RA-5LoLQFgfLMZk3NeIhRRxYx3_6pyyn65_h0UlKvNPww130_assertion wasGeneratedBy ECO_0000218 NP19503.RA-5LoLQFgfLMZk3NeIhRRxYx3_6pyyn65_h0UlKvNPww130_provenance.
- NP19503.RA-5LoLQFgfLMZk3NeIhRRxYx3_6pyyn65_h0UlKvNPww130_assertion wasDerivedFrom ctd_human-20150221 NP19503.RA-5LoLQFgfLMZk3NeIhRRxYx3_6pyyn65_h0UlKvNPww130_provenance.
- NP19503.RA-5LoLQFgfLMZk3NeIhRRxYx3_6pyyn65_h0UlKvNPww130_assertion SIO_000772 18162506 NP19503.RA-5LoLQFgfLMZk3NeIhRRxYx3_6pyyn65_h0UlKvNPww130_provenance.
- NP19503.RA-5LoLQFgfLMZk3NeIhRRxYx3_6pyyn65_h0UlKvNPww130_assertion evidence source_evidence_curated NP19503.RA-5LoLQFgfLMZk3NeIhRRxYx3_6pyyn65_h0UlKvNPww130_provenance.
- NP19503.RA-5LoLQFgfLMZk3NeIhRRxYx3_6pyyn65_h0UlKvNPww130_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." NP19503.RA-5LoLQFgfLMZk3NeIhRRxYx3_6pyyn65_h0UlKvNPww130_provenance.