Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP675901.RATJ8sQ4AaPYZcIiDzDQs5Qg0gE25qnzpW62_FoaT8C1w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP675901.RATJ8sQ4AaPYZcIiDzDQs5Qg0gE25qnzpW62_FoaT8C1w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP675901.RATJ8sQ4AaPYZcIiDzDQs5Qg0gE25qnzpW62_FoaT8C1w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP675901.RATJ8sQ4AaPYZcIiDzDQs5Qg0gE25qnzpW62_FoaT8C1w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP675901.RATJ8sQ4AaPYZcIiDzDQs5Qg0gE25qnzpW62_FoaT8C1w130_provenance.
- NP675901.RATJ8sQ4AaPYZcIiDzDQs5Qg0gE25qnzpW62_FoaT8C1w130_assertion wasGeneratedBy ECO_0000203 NP675901.RATJ8sQ4AaPYZcIiDzDQs5Qg0gE25qnzpW62_FoaT8C1w130_provenance.
- NP675901.RATJ8sQ4AaPYZcIiDzDQs5Qg0gE25qnzpW62_FoaT8C1w130_assertion wasDerivedFrom befree-20150227 NP675901.RATJ8sQ4AaPYZcIiDzDQs5Qg0gE25qnzpW62_FoaT8C1w130_provenance.
- NP675901.RATJ8sQ4AaPYZcIiDzDQs5Qg0gE25qnzpW62_FoaT8C1w130_assertion SIO_000772 21943668 NP675901.RATJ8sQ4AaPYZcIiDzDQs5Qg0gE25qnzpW62_FoaT8C1w130_provenance.
- NP675901.RATJ8sQ4AaPYZcIiDzDQs5Qg0gE25qnzpW62_FoaT8C1w130_assertion evidence source_evidence_literature NP675901.RATJ8sQ4AaPYZcIiDzDQs5Qg0gE25qnzpW62_FoaT8C1w130_provenance.
- NP675901.RATJ8sQ4AaPYZcIiDzDQs5Qg0gE25qnzpW62_FoaT8C1w130_assertion description "[Heterozygous loss of the RPS14 gene on 5q leads to activation of p53 in the erythroid lineage and the macrocytic anemia characteristic of the 5q-syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP675901.RATJ8sQ4AaPYZcIiDzDQs5Qg0gE25qnzpW62_FoaT8C1w130_provenance.