Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_assertion type Assertion NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_head.
- NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_assertion description "[the 35delG mutation was determined as the most frequently shown mutation that leads to congenital hearing loss as in previous studies from Turkey.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_provenance.
- NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_assertion evidence source_evidence_literature NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_provenance.
- NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_assertion SIO_000772 18554165 NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_provenance.
- NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_assertion wasDerivedFrom gad-20150221 NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_provenance.
- NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_assertion wasGeneratedBy ECO_0000203 NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_provenance.