Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294746.RA7bpCZ2QJzNfqR1R3N9cly0YogA5Kt44DBPTeMZ_y2Tc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP294746.RA7bpCZ2QJzNfqR1R3N9cly0YogA5Kt44DBPTeMZ_y2Tc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294746.RA7bpCZ2QJzNfqR1R3N9cly0YogA5Kt44DBPTeMZ_y2Tc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294746.RA7bpCZ2QJzNfqR1R3N9cly0YogA5Kt44DBPTeMZ_y2Tc130_provenance.
- NP294746.RA7bpCZ2QJzNfqR1R3N9cly0YogA5Kt44DBPTeMZ_y2Tc130_assertion description "[Given that mutations in EFEMP1 have been recently described in patients with Doyne honeycomb retinal dystrophy, EFEMP2 becomes a good candidate for such disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294746.RA7bpCZ2QJzNfqR1R3N9cly0YogA5Kt44DBPTeMZ_y2Tc130_provenance.
- NP294746.RA7bpCZ2QJzNfqR1R3N9cly0YogA5Kt44DBPTeMZ_y2Tc130_assertion evidence source_evidence_literature NP294746.RA7bpCZ2QJzNfqR1R3N9cly0YogA5Kt44DBPTeMZ_y2Tc130_provenance.
- NP294746.RA7bpCZ2QJzNfqR1R3N9cly0YogA5Kt44DBPTeMZ_y2Tc130_assertion SIO_000772 10982184 NP294746.RA7bpCZ2QJzNfqR1R3N9cly0YogA5Kt44DBPTeMZ_y2Tc130_provenance.
- NP294746.RA7bpCZ2QJzNfqR1R3N9cly0YogA5Kt44DBPTeMZ_y2Tc130_assertion wasDerivedFrom befree-2016 NP294746.RA7bpCZ2QJzNfqR1R3N9cly0YogA5Kt44DBPTeMZ_y2Tc130_provenance.
- NP294746.RA7bpCZ2QJzNfqR1R3N9cly0YogA5Kt44DBPTeMZ_y2Tc130_assertion wasGeneratedBy ECO_0000203 NP294746.RA7bpCZ2QJzNfqR1R3N9cly0YogA5Kt44DBPTeMZ_y2Tc130_provenance.
- befree-2016 importedOn "2016-02-19" NP294746.RA7bpCZ2QJzNfqR1R3N9cly0YogA5Kt44DBPTeMZ_y2Tc130_provenance.