Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP250364.RAjsH9K31iVgvmiRHc3zrRlEMbdtbYNuoxJoQ4bPQmTzE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP250364.RAjsH9K31iVgvmiRHc3zrRlEMbdtbYNuoxJoQ4bPQmTzE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP250364.RAjsH9K31iVgvmiRHc3zrRlEMbdtbYNuoxJoQ4bPQmTzE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP250364.RAjsH9K31iVgvmiRHc3zrRlEMbdtbYNuoxJoQ4bPQmTzE130_provenance.
- NP250364.RAjsH9K31iVgvmiRHc3zrRlEMbdtbYNuoxJoQ4bPQmTzE130_assertion description "[Clonality investigation including mutational status of MPL, TET2, and ASXL1 genes and human androgen receptor (HUMARA) assay was performed in 73 JAK2V617F-negative cases out of 186 subjects consecutively diagnosed with ET in a single institution, at diagnosis or during follow-up.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP250364.RAjsH9K31iVgvmiRHc3zrRlEMbdtbYNuoxJoQ4bPQmTzE130_provenance.
- NP250364.RAjsH9K31iVgvmiRHc3zrRlEMbdtbYNuoxJoQ4bPQmTzE130_assertion evidence source_evidence_literature NP250364.RAjsH9K31iVgvmiRHc3zrRlEMbdtbYNuoxJoQ4bPQmTzE130_provenance.
- NP250364.RAjsH9K31iVgvmiRHc3zrRlEMbdtbYNuoxJoQ4bPQmTzE130_assertion SIO_000772 22706669 NP250364.RAjsH9K31iVgvmiRHc3zrRlEMbdtbYNuoxJoQ4bPQmTzE130_provenance.
- NP250364.RAjsH9K31iVgvmiRHc3zrRlEMbdtbYNuoxJoQ4bPQmTzE130_assertion wasDerivedFrom befree-20150227 NP250364.RAjsH9K31iVgvmiRHc3zrRlEMbdtbYNuoxJoQ4bPQmTzE130_provenance.
- NP250364.RAjsH9K31iVgvmiRHc3zrRlEMbdtbYNuoxJoQ4bPQmTzE130_assertion wasGeneratedBy ECO_0000203 NP250364.RAjsH9K31iVgvmiRHc3zrRlEMbdtbYNuoxJoQ4bPQmTzE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP250364.RAjsH9K31iVgvmiRHc3zrRlEMbdtbYNuoxJoQ4bPQmTzE130_provenance.