Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1231120.RALmBK9VsIsezScZKUhPiQqKBcF5bHs_wbN1rf-Y1EewU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1231120.RALmBK9VsIsezScZKUhPiQqKBcF5bHs_wbN1rf-Y1EewU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1231120.RALmBK9VsIsezScZKUhPiQqKBcF5bHs_wbN1rf-Y1EewU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1231120.RALmBK9VsIsezScZKUhPiQqKBcF5bHs_wbN1rf-Y1EewU130_provenance.
- NP1231120.RALmBK9VsIsezScZKUhPiQqKBcF5bHs_wbN1rf-Y1EewU130_assertion description "[On the basis of the above results, it was hypothesized that GJB4 may be a genetic risk factor for the development of nonsyndromic hearing loss and the data from the present study can be used to direct the clinical evaluation and effectively manage the care of families of children with GJB4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1231120.RALmBK9VsIsezScZKUhPiQqKBcF5bHs_wbN1rf-Y1EewU130_provenance.
- NP1231120.RALmBK9VsIsezScZKUhPiQqKBcF5bHs_wbN1rf-Y1EewU130_assertion evidence source_evidence_literature NP1231120.RALmBK9VsIsezScZKUhPiQqKBcF5bHs_wbN1rf-Y1EewU130_provenance.
- NP1231120.RALmBK9VsIsezScZKUhPiQqKBcF5bHs_wbN1rf-Y1EewU130_assertion SIO_000772 25333454 NP1231120.RALmBK9VsIsezScZKUhPiQqKBcF5bHs_wbN1rf-Y1EewU130_provenance.
- NP1231120.RALmBK9VsIsezScZKUhPiQqKBcF5bHs_wbN1rf-Y1EewU130_assertion wasDerivedFrom befree-2016 NP1231120.RALmBK9VsIsezScZKUhPiQqKBcF5bHs_wbN1rf-Y1EewU130_provenance.
- NP1231120.RALmBK9VsIsezScZKUhPiQqKBcF5bHs_wbN1rf-Y1EewU130_assertion wasGeneratedBy ECO_0000203 NP1231120.RALmBK9VsIsezScZKUhPiQqKBcF5bHs_wbN1rf-Y1EewU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1231120.RALmBK9VsIsezScZKUhPiQqKBcF5bHs_wbN1rf-Y1EewU130_provenance.