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- source_evidence_literature type ECO_0000212 NP663485.RAyUVy9AZLbijfcfPfpOTKuLE7Rp-hi3IpLEywkyPmn9s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP663485.RAyUVy9AZLbijfcfPfpOTKuLE7Rp-hi3IpLEywkyPmn9s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP663485.RAyUVy9AZLbijfcfPfpOTKuLE7Rp-hi3IpLEywkyPmn9s130_provenance.
- NP663485.RAyUVy9AZLbijfcfPfpOTKuLE7Rp-hi3IpLEywkyPmn9s130_assertion description "[Frequent methylation in NEIL1 (42%) and infrequent methylation in ERCC1 (2%) and RAD23B (2%) are reported for the first time in NSCLC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663485.RAyUVy9AZLbijfcfPfpOTKuLE7Rp-hi3IpLEywkyPmn9s130_provenance.
- NP663485.RAyUVy9AZLbijfcfPfpOTKuLE7Rp-hi3IpLEywkyPmn9s130_assertion evidence source_evidence_literature NP663485.RAyUVy9AZLbijfcfPfpOTKuLE7Rp-hi3IpLEywkyPmn9s130_provenance.
- NP663485.RAyUVy9AZLbijfcfPfpOTKuLE7Rp-hi3IpLEywkyPmn9s130_assertion SIO_000772 24569633 NP663485.RAyUVy9AZLbijfcfPfpOTKuLE7Rp-hi3IpLEywkyPmn9s130_provenance.
- NP663485.RAyUVy9AZLbijfcfPfpOTKuLE7Rp-hi3IpLEywkyPmn9s130_assertion wasDerivedFrom befree-20150227 NP663485.RAyUVy9AZLbijfcfPfpOTKuLE7Rp-hi3IpLEywkyPmn9s130_provenance.
- NP663485.RAyUVy9AZLbijfcfPfpOTKuLE7Rp-hi3IpLEywkyPmn9s130_assertion wasGeneratedBy ECO_0000203 NP663485.RAyUVy9AZLbijfcfPfpOTKuLE7Rp-hi3IpLEywkyPmn9s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP663485.RAyUVy9AZLbijfcfPfpOTKuLE7Rp-hi3IpLEywkyPmn9s130_provenance.