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- NP436669.RA59bUTPYmT0CQ_H6qAFx-C4e5mfaxZ0dSsPPTeVrZcg8130_assertion type Assertion NP436669.RA59bUTPYmT0CQ_H6qAFx-C4e5mfaxZ0dSsPPTeVrZcg8130_head.
- 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.