Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978659.RAWqNvCiivmqIQd20aKmeZpDV1RQ73fKWkAs32GsJY5DM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978659.RAWqNvCiivmqIQd20aKmeZpDV1RQ73fKWkAs32GsJY5DM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978659.RAWqNvCiivmqIQd20aKmeZpDV1RQ73fKWkAs32GsJY5DM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978659.RAWqNvCiivmqIQd20aKmeZpDV1RQ73fKWkAs32GsJY5DM130_provenance.
- NP978659.RAWqNvCiivmqIQd20aKmeZpDV1RQ73fKWkAs32GsJY5DM130_assertion description "[These new data further support ASXL1 as cause of BOS and may contribute to a more precise definition of the phenotype caused by the disruption of this gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978659.RAWqNvCiivmqIQd20aKmeZpDV1RQ73fKWkAs32GsJY5DM130_provenance.
- NP978659.RAWqNvCiivmqIQd20aKmeZpDV1RQ73fKWkAs32GsJY5DM130_assertion evidence source_evidence_literature NP978659.RAWqNvCiivmqIQd20aKmeZpDV1RQ73fKWkAs32GsJY5DM130_provenance.
- NP978659.RAWqNvCiivmqIQd20aKmeZpDV1RQ73fKWkAs32GsJY5DM130_assertion SIO_000772 22419483 NP978659.RAWqNvCiivmqIQd20aKmeZpDV1RQ73fKWkAs32GsJY5DM130_provenance.
- NP978659.RAWqNvCiivmqIQd20aKmeZpDV1RQ73fKWkAs32GsJY5DM130_assertion wasDerivedFrom befree-20150227 NP978659.RAWqNvCiivmqIQd20aKmeZpDV1RQ73fKWkAs32GsJY5DM130_provenance.
- NP978659.RAWqNvCiivmqIQd20aKmeZpDV1RQ73fKWkAs32GsJY5DM130_assertion wasGeneratedBy ECO_0000203 NP978659.RAWqNvCiivmqIQd20aKmeZpDV1RQ73fKWkAs32GsJY5DM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978659.RAWqNvCiivmqIQd20aKmeZpDV1RQ73fKWkAs32GsJY5DM130_provenance.