Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP426460.RALhubq7QG3KOyS3TgAbjWDiueX-uFCNKwraHWTizeG7Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP426460.RALhubq7QG3KOyS3TgAbjWDiueX-uFCNKwraHWTizeG7Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426460.RALhubq7QG3KOyS3TgAbjWDiueX-uFCNKwraHWTizeG7Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426460.RALhubq7QG3KOyS3TgAbjWDiueX-uFCNKwraHWTizeG7Q130_provenance.
- NP426460.RALhubq7QG3KOyS3TgAbjWDiueX-uFCNKwraHWTizeG7Q130_assertion description "[We tested 303 unrelated Czech patients with early hearing loss (298 with NSHL and 5 with PS), all GJB2-negative, for SLC26A4 mutations and evaluated their clinical and radiological phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426460.RALhubq7QG3KOyS3TgAbjWDiueX-uFCNKwraHWTizeG7Q130_provenance.
- NP426460.RALhubq7QG3KOyS3TgAbjWDiueX-uFCNKwraHWTizeG7Q130_assertion evidence source_evidence_literature NP426460.RALhubq7QG3KOyS3TgAbjWDiueX-uFCNKwraHWTizeG7Q130_provenance.
- NP426460.RALhubq7QG3KOyS3TgAbjWDiueX-uFCNKwraHWTizeG7Q130_assertion SIO_000772 20597900 NP426460.RALhubq7QG3KOyS3TgAbjWDiueX-uFCNKwraHWTizeG7Q130_provenance.
- NP426460.RALhubq7QG3KOyS3TgAbjWDiueX-uFCNKwraHWTizeG7Q130_assertion wasDerivedFrom befree-20150227 NP426460.RALhubq7QG3KOyS3TgAbjWDiueX-uFCNKwraHWTizeG7Q130_provenance.
- NP426460.RALhubq7QG3KOyS3TgAbjWDiueX-uFCNKwraHWTizeG7Q130_assertion wasGeneratedBy ECO_0000203 NP426460.RALhubq7QG3KOyS3TgAbjWDiueX-uFCNKwraHWTizeG7Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP426460.RALhubq7QG3KOyS3TgAbjWDiueX-uFCNKwraHWTizeG7Q130_provenance.