Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP552008.RAJszs0kKsFCoz0zYvXliKJP-q7fj5Ll44PcuF-oLsNtc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP552008.RAJszs0kKsFCoz0zYvXliKJP-q7fj5Ll44PcuF-oLsNtc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP552008.RAJszs0kKsFCoz0zYvXliKJP-q7fj5Ll44PcuF-oLsNtc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP552008.RAJszs0kKsFCoz0zYvXliKJP-q7fj5Ll44PcuF-oLsNtc130_provenance.
- NP552008.RAJszs0kKsFCoz0zYvXliKJP-q7fj5Ll44PcuF-oLsNtc130_assertion description "[Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552008.RAJszs0kKsFCoz0zYvXliKJP-q7fj5Ll44PcuF-oLsNtc130_provenance.
- NP552008.RAJszs0kKsFCoz0zYvXliKJP-q7fj5Ll44PcuF-oLsNtc130_assertion evidence source_evidence_literature NP552008.RAJszs0kKsFCoz0zYvXliKJP-q7fj5Ll44PcuF-oLsNtc130_provenance.
- NP552008.RAJszs0kKsFCoz0zYvXliKJP-q7fj5Ll44PcuF-oLsNtc130_assertion SIO_000772 16080119 NP552008.RAJszs0kKsFCoz0zYvXliKJP-q7fj5Ll44PcuF-oLsNtc130_provenance.
- NP552008.RAJszs0kKsFCoz0zYvXliKJP-q7fj5Ll44PcuF-oLsNtc130_assertion wasDerivedFrom befree-20150227 NP552008.RAJszs0kKsFCoz0zYvXliKJP-q7fj5Ll44PcuF-oLsNtc130_provenance.
- NP552008.RAJszs0kKsFCoz0zYvXliKJP-q7fj5Ll44PcuF-oLsNtc130_assertion wasGeneratedBy ECO_0000203 NP552008.RAJszs0kKsFCoz0zYvXliKJP-q7fj5Ll44PcuF-oLsNtc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP552008.RAJszs0kKsFCoz0zYvXliKJP-q7fj5Ll44PcuF-oLsNtc130_provenance.