Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP567323.RAtqIgK1A-c53ommXtq5TpD3vsUNygpd_b8Bo_BKBE3TY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP567323.RAtqIgK1A-c53ommXtq5TpD3vsUNygpd_b8Bo_BKBE3TY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP567323.RAtqIgK1A-c53ommXtq5TpD3vsUNygpd_b8Bo_BKBE3TY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP567323.RAtqIgK1A-c53ommXtq5TpD3vsUNygpd_b8Bo_BKBE3TY130_provenance.
- NP567323.RAtqIgK1A-c53ommXtq5TpD3vsUNygpd_b8Bo_BKBE3TY130_assertion description "[Hereditary thrombocythemia is a rare autosomal dominant disorder caused by mutations in either the thrombopoietin gene (TPO) or its receptor c-MPL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP567323.RAtqIgK1A-c53ommXtq5TpD3vsUNygpd_b8Bo_BKBE3TY130_provenance.
- NP567323.RAtqIgK1A-c53ommXtq5TpD3vsUNygpd_b8Bo_BKBE3TY130_assertion evidence source_evidence_literature NP567323.RAtqIgK1A-c53ommXtq5TpD3vsUNygpd_b8Bo_BKBE3TY130_provenance.
- NP567323.RAtqIgK1A-c53ommXtq5TpD3vsUNygpd_b8Bo_BKBE3TY130_assertion SIO_000772 19553636 NP567323.RAtqIgK1A-c53ommXtq5TpD3vsUNygpd_b8Bo_BKBE3TY130_provenance.
- NP567323.RAtqIgK1A-c53ommXtq5TpD3vsUNygpd_b8Bo_BKBE3TY130_assertion wasDerivedFrom befree-20150227 NP567323.RAtqIgK1A-c53ommXtq5TpD3vsUNygpd_b8Bo_BKBE3TY130_provenance.
- NP567323.RAtqIgK1A-c53ommXtq5TpD3vsUNygpd_b8Bo_BKBE3TY130_assertion wasGeneratedBy ECO_0000203 NP567323.RAtqIgK1A-c53ommXtq5TpD3vsUNygpd_b8Bo_BKBE3TY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP567323.RAtqIgK1A-c53ommXtq5TpD3vsUNygpd_b8Bo_BKBE3TY130_provenance.