Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1245074.RAE_p0S88MnlyI-7Z2Kyc3ZVmHD7HFiffzaW-M70SxpAg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1245074.RAE_p0S88MnlyI-7Z2Kyc3ZVmHD7HFiffzaW-M70SxpAg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1245074.RAE_p0S88MnlyI-7Z2Kyc3ZVmHD7HFiffzaW-M70SxpAg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1245074.RAE_p0S88MnlyI-7Z2Kyc3ZVmHD7HFiffzaW-M70SxpAg130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1245074.RAE_p0S88MnlyI-7Z2Kyc3ZVmHD7HFiffzaW-M70SxpAg130_provenance.