Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP420737.RAuVtcgOPRxZMICNeD0VSh_OpWRGsK9eX9alDxgVe6lg4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP420737.RAuVtcgOPRxZMICNeD0VSh_OpWRGsK9eX9alDxgVe6lg4130_assertion type Assertion NP420737.RAuVtcgOPRxZMICNeD0VSh_OpWRGsK9eX9alDxgVe6lg4130_head.
- NP420737.RAuVtcgOPRxZMICNeD0VSh_OpWRGsK9eX9alDxgVe6lg4130_assertion wasGeneratedBy ECO_0000203 NP420737.RAuVtcgOPRxZMICNeD0VSh_OpWRGsK9eX9alDxgVe6lg4130_provenance.
- NP420737.RAuVtcgOPRxZMICNeD0VSh_OpWRGsK9eX9alDxgVe6lg4130_assertion wasDerivedFrom befree-2016 NP420737.RAuVtcgOPRxZMICNeD0VSh_OpWRGsK9eX9alDxgVe6lg4130_provenance.
- NP420737.RAuVtcgOPRxZMICNeD0VSh_OpWRGsK9eX9alDxgVe6lg4130_assertion SIO_000772 14617022 NP420737.RAuVtcgOPRxZMICNeD0VSh_OpWRGsK9eX9alDxgVe6lg4130_provenance.
- NP420737.RAuVtcgOPRxZMICNeD0VSh_OpWRGsK9eX9alDxgVe6lg4130_assertion evidence source_evidence_literature NP420737.RAuVtcgOPRxZMICNeD0VSh_OpWRGsK9eX9alDxgVe6lg4130_provenance.
- NP420737.RAuVtcgOPRxZMICNeD0VSh_OpWRGsK9eX9alDxgVe6lg4130_assertion description "[Lamin B-receptor mutations in Pelger-Huët anomaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420737.RAuVtcgOPRxZMICNeD0VSh_OpWRGsK9eX9alDxgVe6lg4130_provenance.