Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP604257.RAeb4HCUkv9_caEhAJvyWKisYB0u0ItNSeXrZSV-xbyAA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP604257.RAeb4HCUkv9_caEhAJvyWKisYB0u0ItNSeXrZSV-xbyAA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP604257.RAeb4HCUkv9_caEhAJvyWKisYB0u0ItNSeXrZSV-xbyAA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP604257.RAeb4HCUkv9_caEhAJvyWKisYB0u0ItNSeXrZSV-xbyAA130_provenance.
- NP604257.RAeb4HCUkv9_caEhAJvyWKisYB0u0ItNSeXrZSV-xbyAA130_assertion description "[We also identified one heterozygous 6.5-Mb deletion encompassing OTX2 in a patient with bilateral anophthalmia and multiple pituitary hormone deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP604257.RAeb4HCUkv9_caEhAJvyWKisYB0u0ItNSeXrZSV-xbyAA130_provenance.
- NP604257.RAeb4HCUkv9_caEhAJvyWKisYB0u0ItNSeXrZSV-xbyAA130_assertion evidence source_evidence_literature NP604257.RAeb4HCUkv9_caEhAJvyWKisYB0u0ItNSeXrZSV-xbyAA130_provenance.
- NP604257.RAeb4HCUkv9_caEhAJvyWKisYB0u0ItNSeXrZSV-xbyAA130_assertion SIO_000772 25342853 NP604257.RAeb4HCUkv9_caEhAJvyWKisYB0u0ItNSeXrZSV-xbyAA130_provenance.
- NP604257.RAeb4HCUkv9_caEhAJvyWKisYB0u0ItNSeXrZSV-xbyAA130_assertion wasDerivedFrom befree-20150227 NP604257.RAeb4HCUkv9_caEhAJvyWKisYB0u0ItNSeXrZSV-xbyAA130_provenance.
- NP604257.RAeb4HCUkv9_caEhAJvyWKisYB0u0ItNSeXrZSV-xbyAA130_assertion wasGeneratedBy ECO_0000203 NP604257.RAeb4HCUkv9_caEhAJvyWKisYB0u0ItNSeXrZSV-xbyAA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP604257.RAeb4HCUkv9_caEhAJvyWKisYB0u0ItNSeXrZSV-xbyAA130_provenance.