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- NP209939.RAR4rP-K0u_7EU44pOlcRYGM62W0qhI1fpyl2nLUiwNTw130_assertion type Assertion NP209939.RAR4rP-K0u_7EU44pOlcRYGM62W0qhI1fpyl2nLUiwNTw130_head.
- NP209939.RAR4rP-K0u_7EU44pOlcRYGM62W0qhI1fpyl2nLUiwNTw130_assertion description "[JAK2 V617F mutation that has been associated with 50% of sporadic cases of essential thrombocytopenia was identified as a somatic mutation, an acquired defect, in peripheral blood of the two most severely affected family members ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209939.RAR4rP-K0u_7EU44pOlcRYGM62W0qhI1fpyl2nLUiwNTw130_provenance.
- NP209939.RAR4rP-K0u_7EU44pOlcRYGM62W0qhI1fpyl2nLUiwNTw130_assertion evidence source_evidence_literature NP209939.RAR4rP-K0u_7EU44pOlcRYGM62W0qhI1fpyl2nLUiwNTw130_provenance.
- NP209939.RAR4rP-K0u_7EU44pOlcRYGM62W0qhI1fpyl2nLUiwNTw130_assertion SIO_000772 18496561 NP209939.RAR4rP-K0u_7EU44pOlcRYGM62W0qhI1fpyl2nLUiwNTw130_provenance.
- NP209939.RAR4rP-K0u_7EU44pOlcRYGM62W0qhI1fpyl2nLUiwNTw130_assertion wasDerivedFrom lhgdn-20090331 NP209939.RAR4rP-K0u_7EU44pOlcRYGM62W0qhI1fpyl2nLUiwNTw130_provenance.
- NP209939.RAR4rP-K0u_7EU44pOlcRYGM62W0qhI1fpyl2nLUiwNTw130_assertion wasGeneratedBy ECO_0000203 NP209939.RAR4rP-K0u_7EU44pOlcRYGM62W0qhI1fpyl2nLUiwNTw130_provenance.