Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1245074.RAE_p0S88MnlyI-7Z2Kyc3ZVmHD7HFiffzaW-M70SxpAg130_assertion> ?p ?o ?g. }
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- NP1245074.RAE_p0S88MnlyI-7Z2Kyc3ZVmHD7HFiffzaW-M70SxpAg130_assertion type Assertion NP1245074.RAE_p0S88MnlyI-7Z2Kyc3ZVmHD7HFiffzaW-M70SxpAg130_head.
- NP1245074.RAE_p0S88MnlyI-7Z2Kyc3ZVmHD7HFiffzaW-M70SxpAg130_assertion description "[A previous study showed that a homozygous null allele in NEUROD1 causes severe syndromic disease with neonatal diabetes, systematic neurological abnormalities, and early-onset retinal dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245074.RAE_p0S88MnlyI-7Z2Kyc3ZVmHD7HFiffzaW-M70SxpAg130_provenance.
- NP1245074.RAE_p0S88MnlyI-7Z2Kyc3ZVmHD7HFiffzaW-M70SxpAg130_assertion evidence source_evidence_literature NP1245074.RAE_p0S88MnlyI-7Z2Kyc3ZVmHD7HFiffzaW-M70SxpAg130_provenance.
- NP1245074.RAE_p0S88MnlyI-7Z2Kyc3ZVmHD7HFiffzaW-M70SxpAg130_assertion SIO_000772 25477324 NP1245074.RAE_p0S88MnlyI-7Z2Kyc3ZVmHD7HFiffzaW-M70SxpAg130_provenance.
- NP1245074.RAE_p0S88MnlyI-7Z2Kyc3ZVmHD7HFiffzaW-M70SxpAg130_assertion wasDerivedFrom befree-2016 NP1245074.RAE_p0S88MnlyI-7Z2Kyc3ZVmHD7HFiffzaW-M70SxpAg130_provenance.
- NP1245074.RAE_p0S88MnlyI-7Z2Kyc3ZVmHD7HFiffzaW-M70SxpAg130_assertion wasGeneratedBy ECO_0000203 NP1245074.RAE_p0S88MnlyI-7Z2Kyc3ZVmHD7HFiffzaW-M70SxpAg130_provenance.