Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP391723.RAITUUGAOmrWV3UG3P94WMZUnJc3RnqO3j62ZhpQTrW4E130_assertion> ?p ?o ?g. }
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- NP391723.RAITUUGAOmrWV3UG3P94WMZUnJc3RnqO3j62ZhpQTrW4E130_assertion type Assertion NP391723.RAITUUGAOmrWV3UG3P94WMZUnJc3RnqO3j62ZhpQTrW4E130_head.
- NP391723.RAITUUGAOmrWV3UG3P94WMZUnJc3RnqO3j62ZhpQTrW4E130_assertion description "[We report a rare case of double heterozygous type I protein C deficiency and factor V Leiden in a patient with classic myotonic dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391723.RAITUUGAOmrWV3UG3P94WMZUnJc3RnqO3j62ZhpQTrW4E130_provenance.
- NP391723.RAITUUGAOmrWV3UG3P94WMZUnJc3RnqO3j62ZhpQTrW4E130_assertion evidence source_evidence_literature NP391723.RAITUUGAOmrWV3UG3P94WMZUnJc3RnqO3j62ZhpQTrW4E130_provenance.
- NP391723.RAITUUGAOmrWV3UG3P94WMZUnJc3RnqO3j62ZhpQTrW4E130_assertion SIO_000772 10726006 NP391723.RAITUUGAOmrWV3UG3P94WMZUnJc3RnqO3j62ZhpQTrW4E130_provenance.
- NP391723.RAITUUGAOmrWV3UG3P94WMZUnJc3RnqO3j62ZhpQTrW4E130_assertion wasDerivedFrom befree-20150227 NP391723.RAITUUGAOmrWV3UG3P94WMZUnJc3RnqO3j62ZhpQTrW4E130_provenance.
- NP391723.RAITUUGAOmrWV3UG3P94WMZUnJc3RnqO3j62ZhpQTrW4E130_assertion wasGeneratedBy ECO_0000203 NP391723.RAITUUGAOmrWV3UG3P94WMZUnJc3RnqO3j62ZhpQTrW4E130_provenance.