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- source_evidence_literature type ECO_0000212 NP919933.RAou5u1QDV1QNjAXh7ITv_30IZRkQ8WLJtfOqbf1WeWAc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP919933.RAou5u1QDV1QNjAXh7ITv_30IZRkQ8WLJtfOqbf1WeWAc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP919933.RAou5u1QDV1QNjAXh7ITv_30IZRkQ8WLJtfOqbf1WeWAc130_provenance.
- NP919933.RAou5u1QDV1QNjAXh7ITv_30IZRkQ8WLJtfOqbf1WeWAc130_assertion description "[The aim of our research was to assess the frequency of NBS1 mutations in patients with larynx cancer only (LC) and with MPT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919933.RAou5u1QDV1QNjAXh7ITv_30IZRkQ8WLJtfOqbf1WeWAc130_provenance.
- NP919933.RAou5u1QDV1QNjAXh7ITv_30IZRkQ8WLJtfOqbf1WeWAc130_assertion evidence source_evidence_literature NP919933.RAou5u1QDV1QNjAXh7ITv_30IZRkQ8WLJtfOqbf1WeWAc130_provenance.
- NP919933.RAou5u1QDV1QNjAXh7ITv_30IZRkQ8WLJtfOqbf1WeWAc130_assertion SIO_000772 17894553 NP919933.RAou5u1QDV1QNjAXh7ITv_30IZRkQ8WLJtfOqbf1WeWAc130_provenance.
- NP919933.RAou5u1QDV1QNjAXh7ITv_30IZRkQ8WLJtfOqbf1WeWAc130_assertion wasDerivedFrom befree-20150227 NP919933.RAou5u1QDV1QNjAXh7ITv_30IZRkQ8WLJtfOqbf1WeWAc130_provenance.
- NP919933.RAou5u1QDV1QNjAXh7ITv_30IZRkQ8WLJtfOqbf1WeWAc130_assertion wasGeneratedBy ECO_0000203 NP919933.RAou5u1QDV1QNjAXh7ITv_30IZRkQ8WLJtfOqbf1WeWAc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP919933.RAou5u1QDV1QNjAXh7ITv_30IZRkQ8WLJtfOqbf1WeWAc130_provenance.