Matches in Nanopublications for { ?s ?p "[Glanzmann thrombasthenia is an autosomal recessive bleeding disorder characterized by a life-long hemorrhagic tendency and absent or severely reduced platelet aggregation in response to agonists, caused by quantitative or qualitative abnormalities in the platelet fibrinogen receptor, integrin alphaIIb beta3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP386130.RAT2uTwYzAOYC54BPeYyfjJ59x0FANNJ3MdXou6ozR6wQ130_assertion description "[Glanzmann thrombasthenia is an autosomal recessive bleeding disorder characterized by a life-long hemorrhagic tendency and absent or severely reduced platelet aggregation in response to agonists, caused by quantitative or qualitative abnormalities in the platelet fibrinogen receptor, integrin alphaIIb beta3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP386130.RAT2uTwYzAOYC54BPeYyfjJ59x0FANNJ3MdXou6ozR6wQ130_provenance.
- NP179763.RAGe5bEC0D7Dn9XrPFBSBwwj6Ub5b1aRA2bO3ktcKQXQM130_assertion description "[Glanzmann thrombasthenia is an autosomal recessive bleeding disorder characterized by a life-long hemorrhagic tendency and absent or severely reduced platelet aggregation in response to agonists, caused by quantitative or qualitative abnormalities in the platelet fibrinogen receptor, integrin alphaIIb beta3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179763.RAGe5bEC0D7Dn9XrPFBSBwwj6Ub5b1aRA2bO3ktcKQXQM130_provenance.