Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP552065.RAisUBQ3bF5-YGDxu-bSF5ZNzZO4f7T2wujFbm2GeWT1w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP552065.RAisUBQ3bF5-YGDxu-bSF5ZNzZO4f7T2wujFbm2GeWT1w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP552065.RAisUBQ3bF5-YGDxu-bSF5ZNzZO4f7T2wujFbm2GeWT1w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP552065.RAisUBQ3bF5-YGDxu-bSF5ZNzZO4f7T2wujFbm2GeWT1w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP552065.RAisUBQ3bF5-YGDxu-bSF5ZNzZO4f7T2wujFbm2GeWT1w130_provenance.
- NP552065.RAisUBQ3bF5-YGDxu-bSF5ZNzZO4f7T2wujFbm2GeWT1w130_assertion wasGeneratedBy ECO_0000203 NP552065.RAisUBQ3bF5-YGDxu-bSF5ZNzZO4f7T2wujFbm2GeWT1w130_provenance.
- NP552065.RAisUBQ3bF5-YGDxu-bSF5ZNzZO4f7T2wujFbm2GeWT1w130_assertion wasDerivedFrom befree-20150227 NP552065.RAisUBQ3bF5-YGDxu-bSF5ZNzZO4f7T2wujFbm2GeWT1w130_provenance.
- NP552065.RAisUBQ3bF5-YGDxu-bSF5ZNzZO4f7T2wujFbm2GeWT1w130_assertion SIO_000772 12719401 NP552065.RAisUBQ3bF5-YGDxu-bSF5ZNzZO4f7T2wujFbm2GeWT1w130_provenance.
- NP552065.RAisUBQ3bF5-YGDxu-bSF5ZNzZO4f7T2wujFbm2GeWT1w130_assertion evidence source_evidence_literature NP552065.RAisUBQ3bF5-YGDxu-bSF5ZNzZO4f7T2wujFbm2GeWT1w130_provenance.
- NP552065.RAisUBQ3bF5-YGDxu-bSF5ZNzZO4f7T2wujFbm2GeWT1w130_assertion description "[Neonatal encephalopathy in males is part of a spectrum of disorders caused by MECP2 dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552065.RAisUBQ3bF5-YGDxu-bSF5ZNzZO4f7T2wujFbm2GeWT1w130_provenance.