Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP253.RAbGr3UNvL-i7T37m8df_QdHcAS11C9xYqz_kiXV1_h0Y130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP253.RAbGr3UNvL-i7T37m8df_QdHcAS11C9xYqz_kiXV1_h0Y130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP253.RAbGr3UNvL-i7T37m8df_QdHcAS11C9xYqz_kiXV1_h0Y130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP253.RAbGr3UNvL-i7T37m8df_QdHcAS11C9xYqz_kiXV1_h0Y130_provenance.
- NP253.RAbGr3UNvL-i7T37m8df_QdHcAS11C9xYqz_kiXV1_h0Y130_assertion description "[Best's macular dystrophy (BMD), also known as vitelliform macular degeneration type 2 (VMD2; OMIM 153700), is an autosomal dominant form of macular degeneration with mainly juvenile onset.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253.RAbGr3UNvL-i7T37m8df_QdHcAS11C9xYqz_kiXV1_h0Y130_provenance.
- NP253.RAbGr3UNvL-i7T37m8df_QdHcAS11C9xYqz_kiXV1_h0Y130_assertion evidence source_evidence_curated NP253.RAbGr3UNvL-i7T37m8df_QdHcAS11C9xYqz_kiXV1_h0Y130_provenance.
- NP253.RAbGr3UNvL-i7T37m8df_QdHcAS11C9xYqz_kiXV1_h0Y130_assertion SIO_000772 10394929 NP253.RAbGr3UNvL-i7T37m8df_QdHcAS11C9xYqz_kiXV1_h0Y130_provenance.
- NP253.RAbGr3UNvL-i7T37m8df_QdHcAS11C9xYqz_kiXV1_h0Y130_assertion wasDerivedFrom uniprot-2016 NP253.RAbGr3UNvL-i7T37m8df_QdHcAS11C9xYqz_kiXV1_h0Y130_provenance.
- NP253.RAbGr3UNvL-i7T37m8df_QdHcAS11C9xYqz_kiXV1_h0Y130_assertion wasGeneratedBy ECO_0000218 NP253.RAbGr3UNvL-i7T37m8df_QdHcAS11C9xYqz_kiXV1_h0Y130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP253.RAbGr3UNvL-i7T37m8df_QdHcAS11C9xYqz_kiXV1_h0Y130_provenance.