Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP846250.RAKt8DNTxdlzKtBvT6wHevGATdAMSV-p50Y5VbxDCnqwM130_assertion> ?p ?o ?g. }
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- NP846250.RAKt8DNTxdlzKtBvT6wHevGATdAMSV-p50Y5VbxDCnqwM130_assertion type Assertion NP846250.RAKt8DNTxdlzKtBvT6wHevGATdAMSV-p50Y5VbxDCnqwM130_head.
- NP846250.RAKt8DNTxdlzKtBvT6wHevGATdAMSV-p50Y5VbxDCnqwM130_assertion description "[Germline ASXL1 mutations occur in patients with Bohring-Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP846250.RAKt8DNTxdlzKtBvT6wHevGATdAMSV-p50Y5VbxDCnqwM130_provenance.
- NP846250.RAKt8DNTxdlzKtBvT6wHevGATdAMSV-p50Y5VbxDCnqwM130_assertion evidence source_evidence_literature NP846250.RAKt8DNTxdlzKtBvT6wHevGATdAMSV-p50Y5VbxDCnqwM130_provenance.
- NP846250.RAKt8DNTxdlzKtBvT6wHevGATdAMSV-p50Y5VbxDCnqwM130_assertion SIO_000772 24218140 NP846250.RAKt8DNTxdlzKtBvT6wHevGATdAMSV-p50Y5VbxDCnqwM130_provenance.
- NP846250.RAKt8DNTxdlzKtBvT6wHevGATdAMSV-p50Y5VbxDCnqwM130_assertion wasDerivedFrom befree-20140225 NP846250.RAKt8DNTxdlzKtBvT6wHevGATdAMSV-p50Y5VbxDCnqwM130_provenance.
- NP846250.RAKt8DNTxdlzKtBvT6wHevGATdAMSV-p50Y5VbxDCnqwM130_assertion wasGeneratedBy ECO_0000203 NP846250.RAKt8DNTxdlzKtBvT6wHevGATdAMSV-p50Y5VbxDCnqwM130_provenance.