Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP978689.RAX-Q9_lTxWMfE4R1WUD7yHlH2hTHAFiQGVkmaDUZK6cw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP978689.RAX-Q9_lTxWMfE4R1WUD7yHlH2hTHAFiQGVkmaDUZK6cw130_assertion type Assertion NP978689.RAX-Q9_lTxWMfE4R1WUD7yHlH2hTHAFiQGVkmaDUZK6cw130_head.
- NP978689.RAX-Q9_lTxWMfE4R1WUD7yHlH2hTHAFiQGVkmaDUZK6cw130_assertion description "[De novo ASXL1 mutations cause Bohring-Opitz syndrome characterized by multiple congenital malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978689.RAX-Q9_lTxWMfE4R1WUD7yHlH2hTHAFiQGVkmaDUZK6cw130_provenance.
- NP978689.RAX-Q9_lTxWMfE4R1WUD7yHlH2hTHAFiQGVkmaDUZK6cw130_assertion evidence source_evidence_literature NP978689.RAX-Q9_lTxWMfE4R1WUD7yHlH2hTHAFiQGVkmaDUZK6cw130_provenance.
- NP978689.RAX-Q9_lTxWMfE4R1WUD7yHlH2hTHAFiQGVkmaDUZK6cw130_assertion SIO_000772 24255920 NP978689.RAX-Q9_lTxWMfE4R1WUD7yHlH2hTHAFiQGVkmaDUZK6cw130_provenance.
- NP978689.RAX-Q9_lTxWMfE4R1WUD7yHlH2hTHAFiQGVkmaDUZK6cw130_assertion wasDerivedFrom befree-20150227 NP978689.RAX-Q9_lTxWMfE4R1WUD7yHlH2hTHAFiQGVkmaDUZK6cw130_provenance.
- NP978689.RAX-Q9_lTxWMfE4R1WUD7yHlH2hTHAFiQGVkmaDUZK6cw130_assertion wasGeneratedBy ECO_0000203 NP978689.RAX-Q9_lTxWMfE4R1WUD7yHlH2hTHAFiQGVkmaDUZK6cw130_provenance.