Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_provenance.
- NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_assertion description "[In all, 68 children with nonsyndromic sensorineural hearing loss were screened for Cx26 and Cx30 mutations by polymerase chain reaction and direct sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_provenance.
- NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_assertion evidence source_evidence_literature NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_provenance.
- NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_assertion SIO_000772 15064611 NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_provenance.
- NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_assertion wasDerivedFrom befree-2016 NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_provenance.
- NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_assertion wasGeneratedBy ECO_0000203 NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_provenance.
- befree-2016 importedOn "2016-02-19" NP438352.RACud01f6T2K1U9X9fjcBJ7b9JUkbPIYj7HYwkxvw7ZrE130_provenance.