Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP519094.RAeoQKr9xpFf_8UbNDOidrQiD-LYQDG1U5vH-ts_0OLFc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP519094.RAeoQKr9xpFf_8UbNDOidrQiD-LYQDG1U5vH-ts_0OLFc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP519094.RAeoQKr9xpFf_8UbNDOidrQiD-LYQDG1U5vH-ts_0OLFc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP519094.RAeoQKr9xpFf_8UbNDOidrQiD-LYQDG1U5vH-ts_0OLFc130_provenance.
- NP519094.RAeoQKr9xpFf_8UbNDOidrQiD-LYQDG1U5vH-ts_0OLFc130_assertion description "[This prescient observation was validated by the description of a common mutation in exon 14 of JAK2 for patients with essential thrombocythemia, polycythemia vera and primary myelofibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519094.RAeoQKr9xpFf_8UbNDOidrQiD-LYQDG1U5vH-ts_0OLFc130_provenance.
- NP519094.RAeoQKr9xpFf_8UbNDOidrQiD-LYQDG1U5vH-ts_0OLFc130_assertion evidence source_evidence_literature NP519094.RAeoQKr9xpFf_8UbNDOidrQiD-LYQDG1U5vH-ts_0OLFc130_provenance.
- NP519094.RAeoQKr9xpFf_8UbNDOidrQiD-LYQDG1U5vH-ts_0OLFc130_assertion SIO_000772 24091831 NP519094.RAeoQKr9xpFf_8UbNDOidrQiD-LYQDG1U5vH-ts_0OLFc130_provenance.
- NP519094.RAeoQKr9xpFf_8UbNDOidrQiD-LYQDG1U5vH-ts_0OLFc130_assertion wasDerivedFrom befree-20150227 NP519094.RAeoQKr9xpFf_8UbNDOidrQiD-LYQDG1U5vH-ts_0OLFc130_provenance.
- NP519094.RAeoQKr9xpFf_8UbNDOidrQiD-LYQDG1U5vH-ts_0OLFc130_assertion wasGeneratedBy ECO_0000203 NP519094.RAeoQKr9xpFf_8UbNDOidrQiD-LYQDG1U5vH-ts_0OLFc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP519094.RAeoQKr9xpFf_8UbNDOidrQiD-LYQDG1U5vH-ts_0OLFc130_provenance.