Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_provenance.
- NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_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." NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_provenance.
- NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_assertion evidence source_evidence_literature NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_provenance.
- NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_assertion SIO_000772 22419483 NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_provenance.
- NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_assertion wasDerivedFrom befree-2016 NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_provenance.
- NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_assertion wasGeneratedBy ECO_0000203 NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_provenance.
- befree-2016 importedOn "2016-02-19" NP967817.RAKZ2MjLspcV7yZmUyvyH0QD1bNx0BIL6-UR_4Fg86fFM130_provenance.