Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP691807.RAlwHUwZMChqRMZI1wJ5zI70bmmWENdQXUTnQTWH4wjHE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP691807.RAlwHUwZMChqRMZI1wJ5zI70bmmWENdQXUTnQTWH4wjHE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP691807.RAlwHUwZMChqRMZI1wJ5zI70bmmWENdQXUTnQTWH4wjHE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP691807.RAlwHUwZMChqRMZI1wJ5zI70bmmWENdQXUTnQTWH4wjHE130_provenance.
- befree-2016 importedOn "2016-02-19" NP691807.RAlwHUwZMChqRMZI1wJ5zI70bmmWENdQXUTnQTWH4wjHE130_provenance.
- NP691807.RAlwHUwZMChqRMZI1wJ5zI70bmmWENdQXUTnQTWH4wjHE130_assertion wasGeneratedBy ECO_0000203 NP691807.RAlwHUwZMChqRMZI1wJ5zI70bmmWENdQXUTnQTWH4wjHE130_provenance.
- NP691807.RAlwHUwZMChqRMZI1wJ5zI70bmmWENdQXUTnQTWH4wjHE130_assertion wasDerivedFrom befree-2016 NP691807.RAlwHUwZMChqRMZI1wJ5zI70bmmWENdQXUTnQTWH4wjHE130_provenance.
- NP691807.RAlwHUwZMChqRMZI1wJ5zI70bmmWENdQXUTnQTWH4wjHE130_assertion SIO_000772 18775522 NP691807.RAlwHUwZMChqRMZI1wJ5zI70bmmWENdQXUTnQTWH4wjHE130_provenance.
- NP691807.RAlwHUwZMChqRMZI1wJ5zI70bmmWENdQXUTnQTWH4wjHE130_assertion evidence source_evidence_literature NP691807.RAlwHUwZMChqRMZI1wJ5zI70bmmWENdQXUTnQTWH4wjHE130_provenance.
- NP691807.RAlwHUwZMChqRMZI1wJ5zI70bmmWENdQXUTnQTWH4wjHE130_assertion description "[A 8.26Mb deletion in 6q16 and a 4.95Mb deletion in 20p12 including JAG1 and BMP2 in a patient with Alagille syndrome and Wolff-Parkinson-White syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691807.RAlwHUwZMChqRMZI1wJ5zI70bmmWENdQXUTnQTWH4wjHE130_provenance.