Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP386130.RAT2uTwYzAOYC54BPeYyfjJ59x0FANNJ3MdXou6ozR6wQ130_assertion> ?p ?o ?g. }
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- NP386130.RAT2uTwYzAOYC54BPeYyfjJ59x0FANNJ3MdXou6ozR6wQ130_assertion type Assertion NP386130.RAT2uTwYzAOYC54BPeYyfjJ59x0FANNJ3MdXou6ozR6wQ130_head.
- NP386130.RAT2uTwYzAOYC54BPeYyfjJ59x0FANNJ3MdXou6ozR6wQ130_assertion wasGeneratedBy ECO_0000203 NP386130.RAT2uTwYzAOYC54BPeYyfjJ59x0FANNJ3MdXou6ozR6wQ130_provenance.
- NP386130.RAT2uTwYzAOYC54BPeYyfjJ59x0FANNJ3MdXou6ozR6wQ130_assertion wasDerivedFrom befree-20140225 NP386130.RAT2uTwYzAOYC54BPeYyfjJ59x0FANNJ3MdXou6ozR6wQ130_provenance.
- NP386130.RAT2uTwYzAOYC54BPeYyfjJ59x0FANNJ3MdXou6ozR6wQ130_assertion SIO_000772 17018384 NP386130.RAT2uTwYzAOYC54BPeYyfjJ59x0FANNJ3MdXou6ozR6wQ130_provenance.
- NP386130.RAT2uTwYzAOYC54BPeYyfjJ59x0FANNJ3MdXou6ozR6wQ130_assertion evidence source_evidence_literature NP386130.RAT2uTwYzAOYC54BPeYyfjJ59x0FANNJ3MdXou6ozR6wQ130_provenance.
- 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.