Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1230913.RA6V4ZDw1oOxGi4mku0-55H7LIIrGQWBzBTx_4FwS-yYo130_assertion> ?p ?o ?g. }
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- NP1230913.RA6V4ZDw1oOxGi4mku0-55H7LIIrGQWBzBTx_4FwS-yYo130_assertion type Assertion NP1230913.RA6V4ZDw1oOxGi4mku0-55H7LIIrGQWBzBTx_4FwS-yYo130_head.
- NP1230913.RA6V4ZDw1oOxGi4mku0-55H7LIIrGQWBzBTx_4FwS-yYo130_assertion description "[Whole-exome sequencing identifies a variant in TMEM132E causing autosomal-recessive nonsyndromic hearing loss DFNB99.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1230913.RA6V4ZDw1oOxGi4mku0-55H7LIIrGQWBzBTx_4FwS-yYo130_provenance.
- NP1230913.RA6V4ZDw1oOxGi4mku0-55H7LIIrGQWBzBTx_4FwS-yYo130_assertion evidence source_evidence_literature NP1230913.RA6V4ZDw1oOxGi4mku0-55H7LIIrGQWBzBTx_4FwS-yYo130_provenance.
- NP1230913.RA6V4ZDw1oOxGi4mku0-55H7LIIrGQWBzBTx_4FwS-yYo130_assertion SIO_000772 25331638 NP1230913.RA6V4ZDw1oOxGi4mku0-55H7LIIrGQWBzBTx_4FwS-yYo130_provenance.
- NP1230913.RA6V4ZDw1oOxGi4mku0-55H7LIIrGQWBzBTx_4FwS-yYo130_assertion wasDerivedFrom befree-2016 NP1230913.RA6V4ZDw1oOxGi4mku0-55H7LIIrGQWBzBTx_4FwS-yYo130_provenance.
- NP1230913.RA6V4ZDw1oOxGi4mku0-55H7LIIrGQWBzBTx_4FwS-yYo130_assertion wasGeneratedBy ECO_0000203 NP1230913.RA6V4ZDw1oOxGi4mku0-55H7LIIrGQWBzBTx_4FwS-yYo130_provenance.