Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP580243.RArRU4QPTy2kktjJlsxVXN_tpzX8idQRKn1iMOfefk17Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP580243.RArRU4QPTy2kktjJlsxVXN_tpzX8idQRKn1iMOfefk17Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP580243.RArRU4QPTy2kktjJlsxVXN_tpzX8idQRKn1iMOfefk17Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP580243.RArRU4QPTy2kktjJlsxVXN_tpzX8idQRKn1iMOfefk17Q130_provenance.
- NP580243.RArRU4QPTy2kktjJlsxVXN_tpzX8idQRKn1iMOfefk17Q130_assertion description "[The JAK2 mutation was detected in 25 patients (46%); 12 of 26 patients with essential thrombocythemia (ET), 9 of 12 patients with polycyhtemia vera (PV), one of 7 patients with chronic idiopathic myelofibrosis (CIM) and one patient with unclassifiable MPD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP580243.RArRU4QPTy2kktjJlsxVXN_tpzX8idQRKn1iMOfefk17Q130_provenance.
- NP580243.RArRU4QPTy2kktjJlsxVXN_tpzX8idQRKn1iMOfefk17Q130_assertion evidence source_evidence_literature NP580243.RArRU4QPTy2kktjJlsxVXN_tpzX8idQRKn1iMOfefk17Q130_provenance.
- NP580243.RArRU4QPTy2kktjJlsxVXN_tpzX8idQRKn1iMOfefk17Q130_assertion SIO_000772 17249502 NP580243.RArRU4QPTy2kktjJlsxVXN_tpzX8idQRKn1iMOfefk17Q130_provenance.
- NP580243.RArRU4QPTy2kktjJlsxVXN_tpzX8idQRKn1iMOfefk17Q130_assertion wasDerivedFrom befree-20150227 NP580243.RArRU4QPTy2kktjJlsxVXN_tpzX8idQRKn1iMOfefk17Q130_provenance.
- NP580243.RArRU4QPTy2kktjJlsxVXN_tpzX8idQRKn1iMOfefk17Q130_assertion wasGeneratedBy ECO_0000203 NP580243.RArRU4QPTy2kktjJlsxVXN_tpzX8idQRKn1iMOfefk17Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP580243.RArRU4QPTy2kktjJlsxVXN_tpzX8idQRKn1iMOfefk17Q130_provenance.