Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP14959.RAU81GQi_dAYQNe_486Nu9n3B9jw_owm9d_De2JwwlFW4130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP14959.RAU81GQi_dAYQNe_486Nu9n3B9jw_owm9d_De2JwwlFW4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP14959.RAU81GQi_dAYQNe_486Nu9n3B9jw_owm9d_De2JwwlFW4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP14959.RAU81GQi_dAYQNe_486Nu9n3B9jw_owm9d_De2JwwlFW4130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP14959.RAU81GQi_dAYQNe_486Nu9n3B9jw_owm9d_De2JwwlFW4130_provenance.
- NP14959.RAU81GQi_dAYQNe_486Nu9n3B9jw_owm9d_De2JwwlFW4130_assertion wasGeneratedBy ECO_0000218 NP14959.RAU81GQi_dAYQNe_486Nu9n3B9jw_owm9d_De2JwwlFW4130_provenance.
- NP14959.RAU81GQi_dAYQNe_486Nu9n3B9jw_owm9d_De2JwwlFW4130_assertion wasDerivedFrom ctd_human-20150221 NP14959.RAU81GQi_dAYQNe_486Nu9n3B9jw_owm9d_De2JwwlFW4130_provenance.
- NP14959.RAU81GQi_dAYQNe_486Nu9n3B9jw_owm9d_De2JwwlFW4130_assertion SIO_000772 22043169 NP14959.RAU81GQi_dAYQNe_486Nu9n3B9jw_owm9d_De2JwwlFW4130_provenance.
- NP14959.RAU81GQi_dAYQNe_486Nu9n3B9jw_owm9d_De2JwwlFW4130_assertion evidence source_evidence_curated NP14959.RAU81GQi_dAYQNe_486Nu9n3B9jw_owm9d_De2JwwlFW4130_provenance.
- NP14959.RAU81GQi_dAYQNe_486Nu9n3B9jw_owm9d_De2JwwlFW4130_assertion description "[Fragile x syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP14959.RAU81GQi_dAYQNe_486Nu9n3B9jw_owm9d_De2JwwlFW4130_provenance.