Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP846119.RASzu5QcuP3fKdW8p7E_2_jwDKmiCpd5fxJaRtf-UV-xs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP846119.RASzu5QcuP3fKdW8p7E_2_jwDKmiCpd5fxJaRtf-UV-xs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP846119.RASzu5QcuP3fKdW8p7E_2_jwDKmiCpd5fxJaRtf-UV-xs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP846119.RASzu5QcuP3fKdW8p7E_2_jwDKmiCpd5fxJaRtf-UV-xs130_provenance.
- NP846119.RASzu5QcuP3fKdW8p7E_2_jwDKmiCpd5fxJaRtf-UV-xs130_assertion description "[We investigated whether, in myelodysplastic syndromes (MDS), aberrant expression of miR-150/miR-221/miR-222 and their designated target mRNA molecules MYB, p27 and c-KIT may be involved in insufficient haematopoiesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP846119.RASzu5QcuP3fKdW8p7E_2_jwDKmiCpd5fxJaRtf-UV-xs130_provenance.
- NP846119.RASzu5QcuP3fKdW8p7E_2_jwDKmiCpd5fxJaRtf-UV-xs130_assertion evidence source_evidence_literature NP846119.RASzu5QcuP3fKdW8p7E_2_jwDKmiCpd5fxJaRtf-UV-xs130_provenance.
- NP846119.RASzu5QcuP3fKdW8p7E_2_jwDKmiCpd5fxJaRtf-UV-xs130_assertion SIO_000772 19615744 NP846119.RASzu5QcuP3fKdW8p7E_2_jwDKmiCpd5fxJaRtf-UV-xs130_provenance.
- NP846119.RASzu5QcuP3fKdW8p7E_2_jwDKmiCpd5fxJaRtf-UV-xs130_assertion wasDerivedFrom befree-20150227 NP846119.RASzu5QcuP3fKdW8p7E_2_jwDKmiCpd5fxJaRtf-UV-xs130_provenance.
- NP846119.RASzu5QcuP3fKdW8p7E_2_jwDKmiCpd5fxJaRtf-UV-xs130_assertion wasGeneratedBy ECO_0000203 NP846119.RASzu5QcuP3fKdW8p7E_2_jwDKmiCpd5fxJaRtf-UV-xs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP846119.RASzu5QcuP3fKdW8p7E_2_jwDKmiCpd5fxJaRtf-UV-xs130_provenance.