Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_provenance.
- 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.
- gad-20150221 importedOn "2015-02-21" NP106275.RARFCLV4NCw62ZTppXahMvqJUAMP168sckk881E3AShHU130_provenance.