Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP221922.RAWSSFsYdRAKGYyqwc-JTbruwAPJM2ojAzkkkV2-NSjv0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP221922.RAWSSFsYdRAKGYyqwc-JTbruwAPJM2ojAzkkkV2-NSjv0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP221922.RAWSSFsYdRAKGYyqwc-JTbruwAPJM2ojAzkkkV2-NSjv0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP221922.RAWSSFsYdRAKGYyqwc-JTbruwAPJM2ojAzkkkV2-NSjv0130_provenance.
- NP221922.RAWSSFsYdRAKGYyqwc-JTbruwAPJM2ojAzkkkV2-NSjv0130_assertion description "[These findings strongly suggested that the I122V mutation in ACTG1 caused autosomal dominant non-syndromic hearing impairment in a Chinese family and expanded the spectrum of ACTG1 mutations causing hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221922.RAWSSFsYdRAKGYyqwc-JTbruwAPJM2ojAzkkkV2-NSjv0130_provenance.
- NP221922.RAWSSFsYdRAKGYyqwc-JTbruwAPJM2ojAzkkkV2-NSjv0130_assertion evidence source_evidence_literature NP221922.RAWSSFsYdRAKGYyqwc-JTbruwAPJM2ojAzkkkV2-NSjv0130_provenance.
- NP221922.RAWSSFsYdRAKGYyqwc-JTbruwAPJM2ojAzkkkV2-NSjv0130_assertion SIO_000772 18804074 NP221922.RAWSSFsYdRAKGYyqwc-JTbruwAPJM2ojAzkkkV2-NSjv0130_provenance.
- NP221922.RAWSSFsYdRAKGYyqwc-JTbruwAPJM2ojAzkkkV2-NSjv0130_assertion wasDerivedFrom befree-20150227 NP221922.RAWSSFsYdRAKGYyqwc-JTbruwAPJM2ojAzkkkV2-NSjv0130_provenance.
- NP221922.RAWSSFsYdRAKGYyqwc-JTbruwAPJM2ojAzkkkV2-NSjv0130_assertion wasGeneratedBy ECO_0000203 NP221922.RAWSSFsYdRAKGYyqwc-JTbruwAPJM2ojAzkkkV2-NSjv0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP221922.RAWSSFsYdRAKGYyqwc-JTbruwAPJM2ojAzkkkV2-NSjv0130_provenance.