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- source_evidence_literature type ECO_0000212 NP502604.RAXwzH965l-5aAoN0LQR1DG7Uywx-M395Di-Kf6jOvHOQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP502604.RAXwzH965l-5aAoN0LQR1DG7Uywx-M395Di-Kf6jOvHOQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP502604.RAXwzH965l-5aAoN0LQR1DG7Uywx-M395Di-Kf6jOvHOQ130_provenance.
- NP502604.RAXwzH965l-5aAoN0LQR1DG7Uywx-M395Di-Kf6jOvHOQ130_assertion description "[PCDH19 is expressed in developing brains of human and mouse and is the first member of the cadherin superfamily to be directly implicated in epilepsy or mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502604.RAXwzH965l-5aAoN0LQR1DG7Uywx-M395Di-Kf6jOvHOQ130_provenance.
- NP502604.RAXwzH965l-5aAoN0LQR1DG7Uywx-M395Di-Kf6jOvHOQ130_assertion evidence source_evidence_literature NP502604.RAXwzH965l-5aAoN0LQR1DG7Uywx-M395Di-Kf6jOvHOQ130_provenance.
- NP502604.RAXwzH965l-5aAoN0LQR1DG7Uywx-M395Di-Kf6jOvHOQ130_assertion SIO_000772 18469813 NP502604.RAXwzH965l-5aAoN0LQR1DG7Uywx-M395Di-Kf6jOvHOQ130_provenance.
- NP502604.RAXwzH965l-5aAoN0LQR1DG7Uywx-M395Di-Kf6jOvHOQ130_assertion wasDerivedFrom befree-20140225 NP502604.RAXwzH965l-5aAoN0LQR1DG7Uywx-M395Di-Kf6jOvHOQ130_provenance.
- NP502604.RAXwzH965l-5aAoN0LQR1DG7Uywx-M395Di-Kf6jOvHOQ130_assertion wasGeneratedBy ECO_0000203 NP502604.RAXwzH965l-5aAoN0LQR1DG7Uywx-M395Di-Kf6jOvHOQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP502604.RAXwzH965l-5aAoN0LQR1DG7Uywx-M395Di-Kf6jOvHOQ130_provenance.