Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP211430.RAPOxfyLhlHMlzL3eaZfgRMqcED9QH23nUuk1kb2znaXo130_assertion> ?p ?o ?g. }
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- NP211430.RAPOxfyLhlHMlzL3eaZfgRMqcED9QH23nUuk1kb2znaXo130_assertion type Assertion NP211430.RAPOxfyLhlHMlzL3eaZfgRMqcED9QH23nUuk1kb2znaXo130_head.
- NP211430.RAPOxfyLhlHMlzL3eaZfgRMqcED9QH23nUuk1kb2znaXo130_assertion description "[To provide a complete database of mutations and polymorphisms associated with factor XI deficiency, all available data on hereditary factor XI deficiency from main biological and medical databases were collected ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211430.RAPOxfyLhlHMlzL3eaZfgRMqcED9QH23nUuk1kb2znaXo130_provenance.
- NP211430.RAPOxfyLhlHMlzL3eaZfgRMqcED9QH23nUuk1kb2znaXo130_assertion evidence source_evidence_literature NP211430.RAPOxfyLhlHMlzL3eaZfgRMqcED9QH23nUuk1kb2znaXo130_provenance.
- NP211430.RAPOxfyLhlHMlzL3eaZfgRMqcED9QH23nUuk1kb2znaXo130_assertion SIO_000772 15870541 NP211430.RAPOxfyLhlHMlzL3eaZfgRMqcED9QH23nUuk1kb2znaXo130_provenance.
- NP211430.RAPOxfyLhlHMlzL3eaZfgRMqcED9QH23nUuk1kb2znaXo130_assertion wasDerivedFrom lhgdn-20090331 NP211430.RAPOxfyLhlHMlzL3eaZfgRMqcED9QH23nUuk1kb2znaXo130_provenance.
- NP211430.RAPOxfyLhlHMlzL3eaZfgRMqcED9QH23nUuk1kb2znaXo130_assertion wasGeneratedBy ECO_0000203 NP211430.RAPOxfyLhlHMlzL3eaZfgRMqcED9QH23nUuk1kb2znaXo130_provenance.