Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1298889.RAFsnGUav6q7DlnJqD3o14hFtQruhEUtmEQo5y1JuAG9s130_assertion> ?p ?o ?g. }
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- NP1298889.RAFsnGUav6q7DlnJqD3o14hFtQruhEUtmEQo5y1JuAG9s130_assertion type Assertion NP1298889.RAFsnGUav6q7DlnJqD3o14hFtQruhEUtmEQo5y1JuAG9s130_head.
- NP1298889.RAFsnGUav6q7DlnJqD3o14hFtQruhEUtmEQo5y1JuAG9s130_assertion wasGeneratedBy ECO_0000203 NP1298889.RAFsnGUav6q7DlnJqD3o14hFtQruhEUtmEQo5y1JuAG9s130_provenance.
- NP1298889.RAFsnGUav6q7DlnJqD3o14hFtQruhEUtmEQo5y1JuAG9s130_assertion wasDerivedFrom befree-2016 NP1298889.RAFsnGUav6q7DlnJqD3o14hFtQruhEUtmEQo5y1JuAG9s130_provenance.
- NP1298889.RAFsnGUav6q7DlnJqD3o14hFtQruhEUtmEQo5y1JuAG9s130_assertion SIO_000772 2989700 NP1298889.RAFsnGUav6q7DlnJqD3o14hFtQruhEUtmEQo5y1JuAG9s130_provenance.
- NP1298889.RAFsnGUav6q7DlnJqD3o14hFtQruhEUtmEQo5y1JuAG9s130_assertion evidence source_evidence_literature NP1298889.RAFsnGUav6q7DlnJqD3o14hFtQruhEUtmEQo5y1JuAG9s130_provenance.
- NP1298889.RAFsnGUav6q7DlnJqD3o14hFtQruhEUtmEQo5y1JuAG9s130_assertion description "[Haemophilia B, or Christmas disease, is an inherited X-chromosome-linked bleeding disorder caused by a defect in clotting factor IX and occurs in about 1 in 30,000 males in the United Kingdom.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1298889.RAFsnGUav6q7DlnJqD3o14hFtQruhEUtmEQo5y1JuAG9s130_provenance.