Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP406371.RAspNWhTn0fjVIu82MNMGe4gHyAEdMzDvW7fmIhqKpAVs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP406371.RAspNWhTn0fjVIu82MNMGe4gHyAEdMzDvW7fmIhqKpAVs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP406371.RAspNWhTn0fjVIu82MNMGe4gHyAEdMzDvW7fmIhqKpAVs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP406371.RAspNWhTn0fjVIu82MNMGe4gHyAEdMzDvW7fmIhqKpAVs130_provenance.
- NP406371.RAspNWhTn0fjVIu82MNMGe4gHyAEdMzDvW7fmIhqKpAVs130_assertion description "[We also show that dysmegakaryopoiesis in Fli-1 null embryos resembles that frequently seen in patients with terminal deletions of 11q (Jacobsen or Paris-Trousseau Syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406371.RAspNWhTn0fjVIu82MNMGe4gHyAEdMzDvW7fmIhqKpAVs130_provenance.
- NP406371.RAspNWhTn0fjVIu82MNMGe4gHyAEdMzDvW7fmIhqKpAVs130_assertion evidence source_evidence_literature NP406371.RAspNWhTn0fjVIu82MNMGe4gHyAEdMzDvW7fmIhqKpAVs130_provenance.
- NP406371.RAspNWhTn0fjVIu82MNMGe4gHyAEdMzDvW7fmIhqKpAVs130_assertion SIO_000772 10981960 NP406371.RAspNWhTn0fjVIu82MNMGe4gHyAEdMzDvW7fmIhqKpAVs130_provenance.
- NP406371.RAspNWhTn0fjVIu82MNMGe4gHyAEdMzDvW7fmIhqKpAVs130_assertion wasDerivedFrom befree-20150227 NP406371.RAspNWhTn0fjVIu82MNMGe4gHyAEdMzDvW7fmIhqKpAVs130_provenance.
- NP406371.RAspNWhTn0fjVIu82MNMGe4gHyAEdMzDvW7fmIhqKpAVs130_assertion wasGeneratedBy ECO_0000203 NP406371.RAspNWhTn0fjVIu82MNMGe4gHyAEdMzDvW7fmIhqKpAVs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP406371.RAspNWhTn0fjVIu82MNMGe4gHyAEdMzDvW7fmIhqKpAVs130_provenance.