Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP209017.RABH7C9A3xdTOus38_UoWq7y18ZCuHRXQGU5Fmt1j1ubs130_assertion> ?p ?o ?g. }
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- NP209017.RABH7C9A3xdTOus38_UoWq7y18ZCuHRXQGU5Fmt1j1ubs130_assertion type Assertion NP209017.RABH7C9A3xdTOus38_UoWq7y18ZCuHRXQGU5Fmt1j1ubs130_head.
- NP209017.RABH7C9A3xdTOus38_UoWq7y18ZCuHRXQGU5Fmt1j1ubs130_assertion description "[sequenced the FGF3 gene in 10 unrelated families in which probands had congenital deafness associated with various inner ear anomalies, including Michel aplasia, with or without tooth or external ear anomalies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209017.RABH7C9A3xdTOus38_UoWq7y18ZCuHRXQGU5Fmt1j1ubs130_provenance.
- NP209017.RABH7C9A3xdTOus38_UoWq7y18ZCuHRXQGU5Fmt1j1ubs130_assertion evidence source_evidence_literature NP209017.RABH7C9A3xdTOus38_UoWq7y18ZCuHRXQGU5Fmt1j1ubs130_provenance.
- NP209017.RABH7C9A3xdTOus38_UoWq7y18ZCuHRXQGU5Fmt1j1ubs130_assertion SIO_000772 18435799 NP209017.RABH7C9A3xdTOus38_UoWq7y18ZCuHRXQGU5Fmt1j1ubs130_provenance.
- NP209017.RABH7C9A3xdTOus38_UoWq7y18ZCuHRXQGU5Fmt1j1ubs130_assertion wasDerivedFrom lhgdn-20090331 NP209017.RABH7C9A3xdTOus38_UoWq7y18ZCuHRXQGU5Fmt1j1ubs130_provenance.
- NP209017.RABH7C9A3xdTOus38_UoWq7y18ZCuHRXQGU5Fmt1j1ubs130_assertion wasGeneratedBy ECO_0000203 NP209017.RABH7C9A3xdTOus38_UoWq7y18ZCuHRXQGU5Fmt1j1ubs130_provenance.