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- source_evidence_literature type ECO_0000212 NP715683.RAdO-6RZgnIZUhkquSgvcITwWZcvb9xHyYoXDe9iULPOI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP715683.RAdO-6RZgnIZUhkquSgvcITwWZcvb9xHyYoXDe9iULPOI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP715683.RAdO-6RZgnIZUhkquSgvcITwWZcvb9xHyYoXDe9iULPOI130_provenance.
- NP715683.RAdO-6RZgnIZUhkquSgvcITwWZcvb9xHyYoXDe9iULPOI130_assertion description "[High frequency of connexin26 (GJB2) mutations associated with nonsyndromic hearing loss in the population of Kerala, India.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715683.RAdO-6RZgnIZUhkquSgvcITwWZcvb9xHyYoXDe9iULPOI130_provenance.
- NP715683.RAdO-6RZgnIZUhkquSgvcITwWZcvb9xHyYoXDe9iULPOI130_assertion evidence source_evidence_literature NP715683.RAdO-6RZgnIZUhkquSgvcITwWZcvb9xHyYoXDe9iULPOI130_provenance.
- NP715683.RAdO-6RZgnIZUhkquSgvcITwWZcvb9xHyYoXDe9iULPOI130_assertion SIO_000772 19157576 NP715683.RAdO-6RZgnIZUhkquSgvcITwWZcvb9xHyYoXDe9iULPOI130_provenance.
- NP715683.RAdO-6RZgnIZUhkquSgvcITwWZcvb9xHyYoXDe9iULPOI130_assertion wasDerivedFrom befree-2016 NP715683.RAdO-6RZgnIZUhkquSgvcITwWZcvb9xHyYoXDe9iULPOI130_provenance.
- NP715683.RAdO-6RZgnIZUhkquSgvcITwWZcvb9xHyYoXDe9iULPOI130_assertion wasGeneratedBy ECO_0000203 NP715683.RAdO-6RZgnIZUhkquSgvcITwWZcvb9xHyYoXDe9iULPOI130_provenance.
- befree-2016 importedOn "2016-02-19" NP715683.RAdO-6RZgnIZUhkquSgvcITwWZcvb9xHyYoXDe9iULPOI130_provenance.