Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP426456.RAhUg-pcPN3g-QQT5_ThpNqoJO-OICfaeUhFaXlN7IzxM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP426456.RAhUg-pcPN3g-QQT5_ThpNqoJO-OICfaeUhFaXlN7IzxM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426456.RAhUg-pcPN3g-QQT5_ThpNqoJO-OICfaeUhFaXlN7IzxM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426456.RAhUg-pcPN3g-QQT5_ThpNqoJO-OICfaeUhFaXlN7IzxM130_provenance.
- NP426456.RAhUg-pcPN3g-QQT5_ThpNqoJO-OICfaeUhFaXlN7IzxM130_assertion description "[A total of 133 children from two deaf and hard of hearing pediatric populations were genotyped first for GJB2/6 and, if negative, then for Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426456.RAhUg-pcPN3g-QQT5_ThpNqoJO-OICfaeUhFaXlN7IzxM130_provenance.
- NP426456.RAhUg-pcPN3g-QQT5_ThpNqoJO-OICfaeUhFaXlN7IzxM130_assertion evidence source_evidence_literature NP426456.RAhUg-pcPN3g-QQT5_ThpNqoJO-OICfaeUhFaXlN7IzxM130_provenance.
- NP426456.RAhUg-pcPN3g-QQT5_ThpNqoJO-OICfaeUhFaXlN7IzxM130_assertion SIO_000772 20613545 NP426456.RAhUg-pcPN3g-QQT5_ThpNqoJO-OICfaeUhFaXlN7IzxM130_provenance.
- NP426456.RAhUg-pcPN3g-QQT5_ThpNqoJO-OICfaeUhFaXlN7IzxM130_assertion wasDerivedFrom befree-20150227 NP426456.RAhUg-pcPN3g-QQT5_ThpNqoJO-OICfaeUhFaXlN7IzxM130_provenance.
- NP426456.RAhUg-pcPN3g-QQT5_ThpNqoJO-OICfaeUhFaXlN7IzxM130_assertion wasGeneratedBy ECO_0000203 NP426456.RAhUg-pcPN3g-QQT5_ThpNqoJO-OICfaeUhFaXlN7IzxM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP426456.RAhUg-pcPN3g-QQT5_ThpNqoJO-OICfaeUhFaXlN7IzxM130_provenance.