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- source_evidence_literature type ECO_0000212 NP880795.RAaw_P_JlNbyrbKfhGETmhy-yyGMu35Kj6odwvT_faLww130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP880795.RAaw_P_JlNbyrbKfhGETmhy-yyGMu35Kj6odwvT_faLww130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP880795.RAaw_P_JlNbyrbKfhGETmhy-yyGMu35Kj6odwvT_faLww130_provenance.
- NP880795.RAaw_P_JlNbyrbKfhGETmhy-yyGMu35Kj6odwvT_faLww130_assertion description "[CHMP2B mutations are not a common cause of frontotemporal lobar degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP880795.RAaw_P_JlNbyrbKfhGETmhy-yyGMu35Kj6odwvT_faLww130_provenance.
- NP880795.RAaw_P_JlNbyrbKfhGETmhy-yyGMu35Kj6odwvT_faLww130_assertion evidence source_evidence_literature NP880795.RAaw_P_JlNbyrbKfhGETmhy-yyGMu35Kj6odwvT_faLww130_provenance.
- NP880795.RAaw_P_JlNbyrbKfhGETmhy-yyGMu35Kj6odwvT_faLww130_assertion SIO_000772 16431024 NP880795.RAaw_P_JlNbyrbKfhGETmhy-yyGMu35Kj6odwvT_faLww130_provenance.
- NP880795.RAaw_P_JlNbyrbKfhGETmhy-yyGMu35Kj6odwvT_faLww130_assertion wasDerivedFrom befree-20150227 NP880795.RAaw_P_JlNbyrbKfhGETmhy-yyGMu35Kj6odwvT_faLww130_provenance.
- NP880795.RAaw_P_JlNbyrbKfhGETmhy-yyGMu35Kj6odwvT_faLww130_assertion wasGeneratedBy ECO_0000203 NP880795.RAaw_P_JlNbyrbKfhGETmhy-yyGMu35Kj6odwvT_faLww130_provenance.
- befree-20150227 importedOn "2015-02-27" NP880795.RAaw_P_JlNbyrbKfhGETmhy-yyGMu35Kj6odwvT_faLww130_provenance.