Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP180269.RAs4FYxnPOr9utoMFsoD563e96o8e6VXCjtcBna6x9XbM130_assertion> ?p ?o ?g. }
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- NP180269.RAs4FYxnPOr9utoMFsoD563e96o8e6VXCjtcBna6x9XbM130_assertion type Assertion NP180269.RAs4FYxnPOr9utoMFsoD563e96o8e6VXCjtcBna6x9XbM130_head.
- NP180269.RAs4FYxnPOr9utoMFsoD563e96o8e6VXCjtcBna6x9XbM130_assertion description "[Prospective variants screening of connexin genes in children with hearing impairment: genotype/phenotype correlation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP180269.RAs4FYxnPOr9utoMFsoD563e96o8e6VXCjtcBna6x9XbM130_provenance.
- NP180269.RAs4FYxnPOr9utoMFsoD563e96o8e6VXCjtcBna6x9XbM130_assertion evidence source_evidence_literature NP180269.RAs4FYxnPOr9utoMFsoD563e96o8e6VXCjtcBna6x9XbM130_provenance.
- NP180269.RAs4FYxnPOr9utoMFsoD563e96o8e6VXCjtcBna6x9XbM130_assertion SIO_000772 20593197 NP180269.RAs4FYxnPOr9utoMFsoD563e96o8e6VXCjtcBna6x9XbM130_provenance.
- NP180269.RAs4FYxnPOr9utoMFsoD563e96o8e6VXCjtcBna6x9XbM130_assertion wasDerivedFrom gad-20150221 NP180269.RAs4FYxnPOr9utoMFsoD563e96o8e6VXCjtcBna6x9XbM130_provenance.
- NP180269.RAs4FYxnPOr9utoMFsoD563e96o8e6VXCjtcBna6x9XbM130_assertion wasGeneratedBy ECO_0000203 NP180269.RAs4FYxnPOr9utoMFsoD563e96o8e6VXCjtcBna6x9XbM130_provenance.