Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP872726.RAxFEZdFTMy3b4xK5qd2RBti-MPpltB5WLsRiZXcn4xHE130_assertion> ?p ?o ?g. }
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- NP872726.RAxFEZdFTMy3b4xK5qd2RBti-MPpltB5WLsRiZXcn4xHE130_assertion type Assertion NP872726.RAxFEZdFTMy3b4xK5qd2RBti-MPpltB5WLsRiZXcn4xHE130_head.
- NP872726.RAxFEZdFTMy3b4xK5qd2RBti-MPpltB5WLsRiZXcn4xHE130_assertion description "[Cerebral venous sinus thrombosis is an uncommon condition with many clinical manifestations, and hereditary prothrombotic conditions such as factor Leiden V, deficiency of protein S, protein C and antithrombin III, as well as prothrombin gene mutation, may account for 10-15% of cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872726.RAxFEZdFTMy3b4xK5qd2RBti-MPpltB5WLsRiZXcn4xHE130_provenance.
- NP872726.RAxFEZdFTMy3b4xK5qd2RBti-MPpltB5WLsRiZXcn4xHE130_assertion evidence source_evidence_literature NP872726.RAxFEZdFTMy3b4xK5qd2RBti-MPpltB5WLsRiZXcn4xHE130_provenance.
- NP872726.RAxFEZdFTMy3b4xK5qd2RBti-MPpltB5WLsRiZXcn4xHE130_assertion SIO_000772 17245631 NP872726.RAxFEZdFTMy3b4xK5qd2RBti-MPpltB5WLsRiZXcn4xHE130_provenance.
- NP872726.RAxFEZdFTMy3b4xK5qd2RBti-MPpltB5WLsRiZXcn4xHE130_assertion wasDerivedFrom befree-20140225 NP872726.RAxFEZdFTMy3b4xK5qd2RBti-MPpltB5WLsRiZXcn4xHE130_provenance.
- NP872726.RAxFEZdFTMy3b4xK5qd2RBti-MPpltB5WLsRiZXcn4xHE130_assertion wasGeneratedBy ECO_0000203 NP872726.RAxFEZdFTMy3b4xK5qd2RBti-MPpltB5WLsRiZXcn4xHE130_provenance.