Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP238007.RAzmSdetAIGOXhb4glJumhZ1hh2wCJYDlFyU8mpQO8k1U130_assertion> ?p ?o ?g. }
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- NP238007.RAzmSdetAIGOXhb4glJumhZ1hh2wCJYDlFyU8mpQO8k1U130_assertion type Assertion NP238007.RAzmSdetAIGOXhb4glJumhZ1hh2wCJYDlFyU8mpQO8k1U130_head.
- NP238007.RAzmSdetAIGOXhb4glJumhZ1hh2wCJYDlFyU8mpQO8k1U130_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." NP238007.RAzmSdetAIGOXhb4glJumhZ1hh2wCJYDlFyU8mpQO8k1U130_provenance.
- NP238007.RAzmSdetAIGOXhb4glJumhZ1hh2wCJYDlFyU8mpQO8k1U130_assertion evidence source_evidence_literature NP238007.RAzmSdetAIGOXhb4glJumhZ1hh2wCJYDlFyU8mpQO8k1U130_provenance.
- NP238007.RAzmSdetAIGOXhb4glJumhZ1hh2wCJYDlFyU8mpQO8k1U130_assertion SIO_000772 18496561 NP238007.RAzmSdetAIGOXhb4glJumhZ1hh2wCJYDlFyU8mpQO8k1U130_provenance.
- NP238007.RAzmSdetAIGOXhb4glJumhZ1hh2wCJYDlFyU8mpQO8k1U130_assertion wasDerivedFrom lhgdn-20090331 NP238007.RAzmSdetAIGOXhb4glJumhZ1hh2wCJYDlFyU8mpQO8k1U130_provenance.
- NP238007.RAzmSdetAIGOXhb4glJumhZ1hh2wCJYDlFyU8mpQO8k1U130_assertion wasGeneratedBy ECO_0000203 NP238007.RAzmSdetAIGOXhb4glJumhZ1hh2wCJYDlFyU8mpQO8k1U130_provenance.