Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP378710.RAs8La4TwS3Sgi_uBnlT8V97sIv7z5ssC8_r0LuGluHek130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP378710.RAs8La4TwS3Sgi_uBnlT8V97sIv7z5ssC8_r0LuGluHek130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP378710.RAs8La4TwS3Sgi_uBnlT8V97sIv7z5ssC8_r0LuGluHek130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP378710.RAs8La4TwS3Sgi_uBnlT8V97sIv7z5ssC8_r0LuGluHek130_provenance.
- NP378710.RAs8La4TwS3Sgi_uBnlT8V97sIv7z5ssC8_r0LuGluHek130_assertion wasGeneratedBy ECO_0000203 NP378710.RAs8La4TwS3Sgi_uBnlT8V97sIv7z5ssC8_r0LuGluHek130_provenance.
- NP378710.RAs8La4TwS3Sgi_uBnlT8V97sIv7z5ssC8_r0LuGluHek130_assertion wasDerivedFrom befree-20140225 NP378710.RAs8La4TwS3Sgi_uBnlT8V97sIv7z5ssC8_r0LuGluHek130_provenance.
- NP378710.RAs8La4TwS3Sgi_uBnlT8V97sIv7z5ssC8_r0LuGluHek130_assertion SIO_000772 17875526 NP378710.RAs8La4TwS3Sgi_uBnlT8V97sIv7z5ssC8_r0LuGluHek130_provenance.
- NP378710.RAs8La4TwS3Sgi_uBnlT8V97sIv7z5ssC8_r0LuGluHek130_assertion evidence source_evidence_literature NP378710.RAs8La4TwS3Sgi_uBnlT8V97sIv7z5ssC8_r0LuGluHek130_provenance.
- NP378710.RAs8La4TwS3Sgi_uBnlT8V97sIv7z5ssC8_r0LuGluHek130_assertion description "[We investigated the prevalence of the JAK2 V617F gain-of-function mutation in patients with Philadelphia chromosome-negative chronic myeloproliferative disorders (Ph- MPD) and explored the links between JAK2 mutational status and the clinicopathologic picture of essential thrombocythemia (ET), chronic idiopathic myelofibrosis (CIMF), and polycythemia vera (PV).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP378710.RAs8La4TwS3Sgi_uBnlT8V97sIv7z5ssC8_r0LuGluHek130_provenance.
- befree-20140225 importedOn "2014-02-25" NP378710.RAs8La4TwS3Sgi_uBnlT8V97sIv7z5ssC8_r0LuGluHek130_provenance.