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- source_evidence_literature type ECO_0000212 NP693449.RAzPOBKVmdhqwezexSqkcjAeQRHSPM3INEyZpBCUYTfys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP693449.RAzPOBKVmdhqwezexSqkcjAeQRHSPM3INEyZpBCUYTfys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP693449.RAzPOBKVmdhqwezexSqkcjAeQRHSPM3INEyZpBCUYTfys130_provenance.
- NP693449.RAzPOBKVmdhqwezexSqkcjAeQRHSPM3INEyZpBCUYTfys130_assertion description "[One form of FTD-U, due to mutations in the valosin containing protein (VCP) gene, occurs with an inclusion body myopathy (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693449.RAzPOBKVmdhqwezexSqkcjAeQRHSPM3INEyZpBCUYTfys130_provenance.
- NP693449.RAzPOBKVmdhqwezexSqkcjAeQRHSPM3INEyZpBCUYTfys130_assertion evidence source_evidence_literature NP693449.RAzPOBKVmdhqwezexSqkcjAeQRHSPM3INEyZpBCUYTfys130_provenance.
- NP693449.RAzPOBKVmdhqwezexSqkcjAeQRHSPM3INEyZpBCUYTfys130_assertion SIO_000772 18796596 NP693449.RAzPOBKVmdhqwezexSqkcjAeQRHSPM3INEyZpBCUYTfys130_provenance.
- NP693449.RAzPOBKVmdhqwezexSqkcjAeQRHSPM3INEyZpBCUYTfys130_assertion wasDerivedFrom befree-2016 NP693449.RAzPOBKVmdhqwezexSqkcjAeQRHSPM3INEyZpBCUYTfys130_provenance.
- NP693449.RAzPOBKVmdhqwezexSqkcjAeQRHSPM3INEyZpBCUYTfys130_assertion wasGeneratedBy ECO_0000203 NP693449.RAzPOBKVmdhqwezexSqkcjAeQRHSPM3INEyZpBCUYTfys130_provenance.
- befree-2016 importedOn "2016-02-19" NP693449.RAzPOBKVmdhqwezexSqkcjAeQRHSPM3INEyZpBCUYTfys130_provenance.