Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP436669.RA59bUTPYmT0CQ_H6qAFx-C4e5mfaxZ0dSsPPTeVrZcg8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP436669.RA59bUTPYmT0CQ_H6qAFx-C4e5mfaxZ0dSsPPTeVrZcg8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP436669.RA59bUTPYmT0CQ_H6qAFx-C4e5mfaxZ0dSsPPTeVrZcg8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP436669.RA59bUTPYmT0CQ_H6qAFx-C4e5mfaxZ0dSsPPTeVrZcg8130_provenance.
- NP436669.RA59bUTPYmT0CQ_H6qAFx-C4e5mfaxZ0dSsPPTeVrZcg8130_assertion description "[Main outcome measure: Presence or absence of mutation in PHOX2A gene in two siblings with exotropia and recessive CFEOM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP436669.RA59bUTPYmT0CQ_H6qAFx-C4e5mfaxZ0dSsPPTeVrZcg8130_provenance.
- NP436669.RA59bUTPYmT0CQ_H6qAFx-C4e5mfaxZ0dSsPPTeVrZcg8130_assertion evidence source_evidence_literature NP436669.RA59bUTPYmT0CQ_H6qAFx-C4e5mfaxZ0dSsPPTeVrZcg8130_provenance.
- NP436669.RA59bUTPYmT0CQ_H6qAFx-C4e5mfaxZ0dSsPPTeVrZcg8130_assertion SIO_000772 14597037 NP436669.RA59bUTPYmT0CQ_H6qAFx-C4e5mfaxZ0dSsPPTeVrZcg8130_provenance.
- NP436669.RA59bUTPYmT0CQ_H6qAFx-C4e5mfaxZ0dSsPPTeVrZcg8130_assertion wasDerivedFrom befree-20140225 NP436669.RA59bUTPYmT0CQ_H6qAFx-C4e5mfaxZ0dSsPPTeVrZcg8130_provenance.
- NP436669.RA59bUTPYmT0CQ_H6qAFx-C4e5mfaxZ0dSsPPTeVrZcg8130_assertion wasGeneratedBy ECO_0000203 NP436669.RA59bUTPYmT0CQ_H6qAFx-C4e5mfaxZ0dSsPPTeVrZcg8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP436669.RA59bUTPYmT0CQ_H6qAFx-C4e5mfaxZ0dSsPPTeVrZcg8130_provenance.