Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP216492.RATqFKT-ec4sjPzeAm4eqTUQHzqKUbDFX-BpLydwm6Lik130_assertion> ?p ?o ?g. }
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- NP216492.RATqFKT-ec4sjPzeAm4eqTUQHzqKUbDFX-BpLydwm6Lik130_assertion type Assertion NP216492.RATqFKT-ec4sjPzeAm4eqTUQHzqKUbDFX-BpLydwm6Lik130_head.
- NP216492.RATqFKT-ec4sjPzeAm4eqTUQHzqKUbDFX-BpLydwm6Lik130_assertion description "[three new exonic LHX4 allelic variants with at least one being responsible for congenital hypopituitarism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216492.RATqFKT-ec4sjPzeAm4eqTUQHzqKUbDFX-BpLydwm6Lik130_provenance.
- NP216492.RATqFKT-ec4sjPzeAm4eqTUQHzqKUbDFX-BpLydwm6Lik130_assertion evidence source_evidence_literature NP216492.RATqFKT-ec4sjPzeAm4eqTUQHzqKUbDFX-BpLydwm6Lik130_provenance.
- NP216492.RATqFKT-ec4sjPzeAm4eqTUQHzqKUbDFX-BpLydwm6Lik130_assertion SIO_000772 18445675 NP216492.RATqFKT-ec4sjPzeAm4eqTUQHzqKUbDFX-BpLydwm6Lik130_provenance.
- NP216492.RATqFKT-ec4sjPzeAm4eqTUQHzqKUbDFX-BpLydwm6Lik130_assertion wasDerivedFrom lhgdn-20090331 NP216492.RATqFKT-ec4sjPzeAm4eqTUQHzqKUbDFX-BpLydwm6Lik130_provenance.
- NP216492.RATqFKT-ec4sjPzeAm4eqTUQHzqKUbDFX-BpLydwm6Lik130_assertion wasGeneratedBy ECO_0000203 NP216492.RATqFKT-ec4sjPzeAm4eqTUQHzqKUbDFX-BpLydwm6Lik130_provenance.