Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP239299.RASAGnADj_WimCaqfbca_bMQvcuIrKkLTS6Rug5k1Xeqo130_assertion> ?p ?o ?g. }
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- NP239299.RASAGnADj_WimCaqfbca_bMQvcuIrKkLTS6Rug5k1Xeqo130_assertion type Assertion NP239299.RASAGnADj_WimCaqfbca_bMQvcuIrKkLTS6Rug5k1Xeqo130_head.
- NP239299.RASAGnADj_WimCaqfbca_bMQvcuIrKkLTS6Rug5k1Xeqo130_assertion wasGeneratedBy ECO_0000203 NP239299.RASAGnADj_WimCaqfbca_bMQvcuIrKkLTS6Rug5k1Xeqo130_provenance.
- NP239299.RASAGnADj_WimCaqfbca_bMQvcuIrKkLTS6Rug5k1Xeqo130_assertion wasDerivedFrom befree-20140225 NP239299.RASAGnADj_WimCaqfbca_bMQvcuIrKkLTS6Rug5k1Xeqo130_provenance.
- NP239299.RASAGnADj_WimCaqfbca_bMQvcuIrKkLTS6Rug5k1Xeqo130_assertion SIO_000772 2989700 NP239299.RASAGnADj_WimCaqfbca_bMQvcuIrKkLTS6Rug5k1Xeqo130_provenance.
- NP239299.RASAGnADj_WimCaqfbca_bMQvcuIrKkLTS6Rug5k1Xeqo130_assertion evidence source_evidence_literature NP239299.RASAGnADj_WimCaqfbca_bMQvcuIrKkLTS6Rug5k1Xeqo130_provenance.
- NP239299.RASAGnADj_WimCaqfbca_bMQvcuIrKkLTS6Rug5k1Xeqo130_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." NP239299.RASAGnADj_WimCaqfbca_bMQvcuIrKkLTS6Rug5k1Xeqo130_provenance.