Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP31540.RAp3p_shMjbEpvvRdP4tSgIDqcM3T8VwOeV91cjemj1WY130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP31540.RAp3p_shMjbEpvvRdP4tSgIDqcM3T8VwOeV91cjemj1WY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP31540.RAp3p_shMjbEpvvRdP4tSgIDqcM3T8VwOeV91cjemj1WY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP31540.RAp3p_shMjbEpvvRdP4tSgIDqcM3T8VwOeV91cjemj1WY130_provenance.
- NP31540.RAp3p_shMjbEpvvRdP4tSgIDqcM3T8VwOeV91cjemj1WY130_assertion description "[Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP31540.RAp3p_shMjbEpvvRdP4tSgIDqcM3T8VwOeV91cjemj1WY130_provenance.
- NP31540.RAp3p_shMjbEpvvRdP4tSgIDqcM3T8VwOeV91cjemj1WY130_assertion evidence source_evidence_curated NP31540.RAp3p_shMjbEpvvRdP4tSgIDqcM3T8VwOeV91cjemj1WY130_provenance.
- NP31540.RAp3p_shMjbEpvvRdP4tSgIDqcM3T8VwOeV91cjemj1WY130_assertion SIO_000772 23708187 NP31540.RAp3p_shMjbEpvvRdP4tSgIDqcM3T8VwOeV91cjemj1WY130_provenance.
- NP31540.RAp3p_shMjbEpvvRdP4tSgIDqcM3T8VwOeV91cjemj1WY130_assertion wasDerivedFrom ctd_human-20150221 NP31540.RAp3p_shMjbEpvvRdP4tSgIDqcM3T8VwOeV91cjemj1WY130_provenance.
- NP31540.RAp3p_shMjbEpvvRdP4tSgIDqcM3T8VwOeV91cjemj1WY130_assertion wasGeneratedBy ECO_0000218 NP31540.RAp3p_shMjbEpvvRdP4tSgIDqcM3T8VwOeV91cjemj1WY130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP31540.RAp3p_shMjbEpvvRdP4tSgIDqcM3T8VwOeV91cjemj1WY130_provenance.