Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP329814.RArhDeJ9FBiJFBIPpd0afotifLTmhsDBh_vlZg3F0dTQM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP329814.RArhDeJ9FBiJFBIPpd0afotifLTmhsDBh_vlZg3F0dTQM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP329814.RArhDeJ9FBiJFBIPpd0afotifLTmhsDBh_vlZg3F0dTQM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP329814.RArhDeJ9FBiJFBIPpd0afotifLTmhsDBh_vlZg3F0dTQM130_provenance.
- NP329814.RArhDeJ9FBiJFBIPpd0afotifLTmhsDBh_vlZg3F0dTQM130_assertion description "[Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329814.RArhDeJ9FBiJFBIPpd0afotifLTmhsDBh_vlZg3F0dTQM130_provenance.
- NP329814.RArhDeJ9FBiJFBIPpd0afotifLTmhsDBh_vlZg3F0dTQM130_assertion evidence source_evidence_literature NP329814.RArhDeJ9FBiJFBIPpd0afotifLTmhsDBh_vlZg3F0dTQM130_provenance.
- NP329814.RArhDeJ9FBiJFBIPpd0afotifLTmhsDBh_vlZg3F0dTQM130_assertion SIO_000772 1829836 NP329814.RArhDeJ9FBiJFBIPpd0afotifLTmhsDBh_vlZg3F0dTQM130_provenance.
- NP329814.RArhDeJ9FBiJFBIPpd0afotifLTmhsDBh_vlZg3F0dTQM130_assertion wasDerivedFrom befree-20150227 NP329814.RArhDeJ9FBiJFBIPpd0afotifLTmhsDBh_vlZg3F0dTQM130_provenance.
- NP329814.RArhDeJ9FBiJFBIPpd0afotifLTmhsDBh_vlZg3F0dTQM130_assertion wasGeneratedBy ECO_0000203 NP329814.RArhDeJ9FBiJFBIPpd0afotifLTmhsDBh_vlZg3F0dTQM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP329814.RArhDeJ9FBiJFBIPpd0afotifLTmhsDBh_vlZg3F0dTQM130_provenance.