Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1293079.RAOHcL-eQbP9zq_BKwKdkJ4owbJPsN2wJzmDM9j_hMlHg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1293079.RAOHcL-eQbP9zq_BKwKdkJ4owbJPsN2wJzmDM9j_hMlHg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293079.RAOHcL-eQbP9zq_BKwKdkJ4owbJPsN2wJzmDM9j_hMlHg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293079.RAOHcL-eQbP9zq_BKwKdkJ4owbJPsN2wJzmDM9j_hMlHg130_provenance.
- NP1293079.RAOHcL-eQbP9zq_BKwKdkJ4owbJPsN2wJzmDM9j_hMlHg130_assertion description "[Because RBPJ, NOTCH1, and EOGT are involved in NOTCH signaling, we hypothesized that mutations in other genes involved in this pathway might also be implicated in AOS pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293079.RAOHcL-eQbP9zq_BKwKdkJ4owbJPsN2wJzmDM9j_hMlHg130_provenance.
- NP1293079.RAOHcL-eQbP9zq_BKwKdkJ4owbJPsN2wJzmDM9j_hMlHg130_assertion evidence source_evidence_literature NP1293079.RAOHcL-eQbP9zq_BKwKdkJ4owbJPsN2wJzmDM9j_hMlHg130_provenance.
- NP1293079.RAOHcL-eQbP9zq_BKwKdkJ4owbJPsN2wJzmDM9j_hMlHg130_assertion SIO_000772 26299364 NP1293079.RAOHcL-eQbP9zq_BKwKdkJ4owbJPsN2wJzmDM9j_hMlHg130_provenance.
- NP1293079.RAOHcL-eQbP9zq_BKwKdkJ4owbJPsN2wJzmDM9j_hMlHg130_assertion wasDerivedFrom befree-2016 NP1293079.RAOHcL-eQbP9zq_BKwKdkJ4owbJPsN2wJzmDM9j_hMlHg130_provenance.
- NP1293079.RAOHcL-eQbP9zq_BKwKdkJ4owbJPsN2wJzmDM9j_hMlHg130_assertion wasGeneratedBy ECO_0000203 NP1293079.RAOHcL-eQbP9zq_BKwKdkJ4owbJPsN2wJzmDM9j_hMlHg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293079.RAOHcL-eQbP9zq_BKwKdkJ4owbJPsN2wJzmDM9j_hMlHg130_provenance.