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- source_evidence_literature type ECO_0000212 NP824361.RABoKjZQbESox-M1hbUxamseKOETiP8n1OF692-ebuMsM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP824361.RABoKjZQbESox-M1hbUxamseKOETiP8n1OF692-ebuMsM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP824361.RABoKjZQbESox-M1hbUxamseKOETiP8n1OF692-ebuMsM130_provenance.
- NP824361.RABoKjZQbESox-M1hbUxamseKOETiP8n1OF692-ebuMsM130_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." NP824361.RABoKjZQbESox-M1hbUxamseKOETiP8n1OF692-ebuMsM130_provenance.
- NP824361.RABoKjZQbESox-M1hbUxamseKOETiP8n1OF692-ebuMsM130_assertion evidence source_evidence_literature NP824361.RABoKjZQbESox-M1hbUxamseKOETiP8n1OF692-ebuMsM130_provenance.
- NP824361.RABoKjZQbESox-M1hbUxamseKOETiP8n1OF692-ebuMsM130_assertion SIO_000772 20613545 NP824361.RABoKjZQbESox-M1hbUxamseKOETiP8n1OF692-ebuMsM130_provenance.
- NP824361.RABoKjZQbESox-M1hbUxamseKOETiP8n1OF692-ebuMsM130_assertion wasDerivedFrom befree-2016 NP824361.RABoKjZQbESox-M1hbUxamseKOETiP8n1OF692-ebuMsM130_provenance.
- NP824361.RABoKjZQbESox-M1hbUxamseKOETiP8n1OF692-ebuMsM130_assertion wasGeneratedBy ECO_0000203 NP824361.RABoKjZQbESox-M1hbUxamseKOETiP8n1OF692-ebuMsM130_provenance.
- befree-2016 importedOn "2016-02-19" NP824361.RABoKjZQbESox-M1hbUxamseKOETiP8n1OF692-ebuMsM130_provenance.