Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP399152.RA6PbrGj1XR8clQbazZFWXpC0M8QcniE5EQNZgmGId67g130_assertion> ?p ?o ?g. }
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- NP399152.RA6PbrGj1XR8clQbazZFWXpC0M8QcniE5EQNZgmGId67g130_assertion type Assertion NP399152.RA6PbrGj1XR8clQbazZFWXpC0M8QcniE5EQNZgmGId67g130_head.
- NP399152.RA6PbrGj1XR8clQbazZFWXpC0M8QcniE5EQNZgmGId67g130_assertion description "[In order to better characterize the phenotypic spectrum associated with FGF3 mutations, we 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." NP399152.RA6PbrGj1XR8clQbazZFWXpC0M8QcniE5EQNZgmGId67g130_provenance.
- NP399152.RA6PbrGj1XR8clQbazZFWXpC0M8QcniE5EQNZgmGId67g130_assertion evidence source_evidence_literature NP399152.RA6PbrGj1XR8clQbazZFWXpC0M8QcniE5EQNZgmGId67g130_provenance.
- NP399152.RA6PbrGj1XR8clQbazZFWXpC0M8QcniE5EQNZgmGId67g130_assertion SIO_000772 18435799 NP399152.RA6PbrGj1XR8clQbazZFWXpC0M8QcniE5EQNZgmGId67g130_provenance.
- NP399152.RA6PbrGj1XR8clQbazZFWXpC0M8QcniE5EQNZgmGId67g130_assertion wasDerivedFrom befree-20150227 NP399152.RA6PbrGj1XR8clQbazZFWXpC0M8QcniE5EQNZgmGId67g130_provenance.
- NP399152.RA6PbrGj1XR8clQbazZFWXpC0M8QcniE5EQNZgmGId67g130_assertion wasGeneratedBy ECO_0000203 NP399152.RA6PbrGj1XR8clQbazZFWXpC0M8QcniE5EQNZgmGId67g130_provenance.