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- NP444401.RAleywQbvMcdsetfAMl26r4RQan8_rTL9JcQzMfZSAb4g130_assertion type Assertion NP444401.RAleywQbvMcdsetfAMl26r4RQan8_rTL9JcQzMfZSAb4g130_head.
- NP444401.RAleywQbvMcdsetfAMl26r4RQan8_rTL9JcQzMfZSAb4g130_assertion description "[BOR syndrome is an autosomal dominant trait encompassing branchial, otic and renal anomalies because of mutations in EYA1, SIX1 and SIX5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444401.RAleywQbvMcdsetfAMl26r4RQan8_rTL9JcQzMfZSAb4g130_provenance.
- NP444401.RAleywQbvMcdsetfAMl26r4RQan8_rTL9JcQzMfZSAb4g130_assertion evidence source_evidence_literature NP444401.RAleywQbvMcdsetfAMl26r4RQan8_rTL9JcQzMfZSAb4g130_provenance.
- NP444401.RAleywQbvMcdsetfAMl26r4RQan8_rTL9JcQzMfZSAb4g130_assertion SIO_000772 18177466 NP444401.RAleywQbvMcdsetfAMl26r4RQan8_rTL9JcQzMfZSAb4g130_provenance.
- NP444401.RAleywQbvMcdsetfAMl26r4RQan8_rTL9JcQzMfZSAb4g130_assertion wasDerivedFrom befree-20140225 NP444401.RAleywQbvMcdsetfAMl26r4RQan8_rTL9JcQzMfZSAb4g130_provenance.
- NP444401.RAleywQbvMcdsetfAMl26r4RQan8_rTL9JcQzMfZSAb4g130_assertion wasGeneratedBy ECO_0000203 NP444401.RAleywQbvMcdsetfAMl26r4RQan8_rTL9JcQzMfZSAb4g130_provenance.