Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP699268.RA5ZmQuFwpFacwuvt-xZCw1UOoVWtvnx6ZT9WsNA2s_cg130_assertion> ?p ?o ?g. }
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- NP699268.RA5ZmQuFwpFacwuvt-xZCw1UOoVWtvnx6ZT9WsNA2s_cg130_assertion type Assertion NP699268.RA5ZmQuFwpFacwuvt-xZCw1UOoVWtvnx6ZT9WsNA2s_cg130_head.
- NP699268.RA5ZmQuFwpFacwuvt-xZCw1UOoVWtvnx6ZT9WsNA2s_cg130_assertion wasGeneratedBy ECO_0000203 NP699268.RA5ZmQuFwpFacwuvt-xZCw1UOoVWtvnx6ZT9WsNA2s_cg130_provenance.
- NP699268.RA5ZmQuFwpFacwuvt-xZCw1UOoVWtvnx6ZT9WsNA2s_cg130_assertion wasDerivedFrom befree-2016 NP699268.RA5ZmQuFwpFacwuvt-xZCw1UOoVWtvnx6ZT9WsNA2s_cg130_provenance.
- NP699268.RA5ZmQuFwpFacwuvt-xZCw1UOoVWtvnx6ZT9WsNA2s_cg130_assertion SIO_000772 18941476 NP699268.RA5ZmQuFwpFacwuvt-xZCw1UOoVWtvnx6ZT9WsNA2s_cg130_provenance.
- NP699268.RA5ZmQuFwpFacwuvt-xZCw1UOoVWtvnx6ZT9WsNA2s_cg130_assertion evidence source_evidence_literature NP699268.RA5ZmQuFwpFacwuvt-xZCw1UOoVWtvnx6ZT9WsNA2s_cg130_provenance.
- NP699268.RA5ZmQuFwpFacwuvt-xZCw1UOoVWtvnx6ZT9WsNA2s_cg130_assertion description "[Functional consequences of novel connexin 26 mutations associated with hereditary hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699268.RA5ZmQuFwpFacwuvt-xZCw1UOoVWtvnx6ZT9WsNA2s_cg130_provenance.