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- source_evidence_literature type ECO_0000212 NP294744.RAnRgnZk7ob4xjwJEIoHyJhZ_i8ZJqMknRxHEzrLSNbFM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294744.RAnRgnZk7ob4xjwJEIoHyJhZ_i8ZJqMknRxHEzrLSNbFM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294744.RAnRgnZk7ob4xjwJEIoHyJhZ_i8ZJqMknRxHEzrLSNbFM130_provenance.
- NP294744.RAnRgnZk7ob4xjwJEIoHyJhZ_i8ZJqMknRxHEzrLSNbFM130_assertion description "[The entire coding region of connexin 26 was sequenced in 75 hearing impaired children and adults in Israel in order to determine the percentage of hearing loss attributed to connexin 26 and the types of mutations in this population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294744.RAnRgnZk7ob4xjwJEIoHyJhZ_i8ZJqMknRxHEzrLSNbFM130_provenance.
- NP294744.RAnRgnZk7ob4xjwJEIoHyJhZ_i8ZJqMknRxHEzrLSNbFM130_assertion evidence source_evidence_literature NP294744.RAnRgnZk7ob4xjwJEIoHyJhZ_i8ZJqMknRxHEzrLSNbFM130_provenance.
- NP294744.RAnRgnZk7ob4xjwJEIoHyJhZ_i8ZJqMknRxHEzrLSNbFM130_assertion SIO_000772 10982182 NP294744.RAnRgnZk7ob4xjwJEIoHyJhZ_i8ZJqMknRxHEzrLSNbFM130_provenance.
- NP294744.RAnRgnZk7ob4xjwJEIoHyJhZ_i8ZJqMknRxHEzrLSNbFM130_assertion wasDerivedFrom befree-2016 NP294744.RAnRgnZk7ob4xjwJEIoHyJhZ_i8ZJqMknRxHEzrLSNbFM130_provenance.
- NP294744.RAnRgnZk7ob4xjwJEIoHyJhZ_i8ZJqMknRxHEzrLSNbFM130_assertion wasGeneratedBy ECO_0000203 NP294744.RAnRgnZk7ob4xjwJEIoHyJhZ_i8ZJqMknRxHEzrLSNbFM130_provenance.
- befree-2016 importedOn "2016-02-19" NP294744.RAnRgnZk7ob4xjwJEIoHyJhZ_i8ZJqMknRxHEzrLSNbFM130_provenance.