Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP781590.RAUQ_ibP-B_oYTEL8GHNArNslU3S0sz_gO9alvS-F2x-E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP781590.RAUQ_ibP-B_oYTEL8GHNArNslU3S0sz_gO9alvS-F2x-E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781590.RAUQ_ibP-B_oYTEL8GHNArNslU3S0sz_gO9alvS-F2x-E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781590.RAUQ_ibP-B_oYTEL8GHNArNslU3S0sz_gO9alvS-F2x-E130_provenance.
- NP781590.RAUQ_ibP-B_oYTEL8GHNArNslU3S0sz_gO9alvS-F2x-E130_assertion description "[The BCR-ABL-negative chronic myeloproliferative disorders (CMPD) and myelodysplastic/myeloproliferative diseases (MDS/MPD) are a spectrum of related conditions for which the molecular pathogenesis is poorly understood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781590.RAUQ_ibP-B_oYTEL8GHNArNslU3S0sz_gO9alvS-F2x-E130_provenance.
- NP781590.RAUQ_ibP-B_oYTEL8GHNArNslU3S0sz_gO9alvS-F2x-E130_assertion evidence source_evidence_literature NP781590.RAUQ_ibP-B_oYTEL8GHNArNslU3S0sz_gO9alvS-F2x-E130_provenance.
- NP781590.RAUQ_ibP-B_oYTEL8GHNArNslU3S0sz_gO9alvS-F2x-E130_assertion SIO_000772 12542482 NP781590.RAUQ_ibP-B_oYTEL8GHNArNslU3S0sz_gO9alvS-F2x-E130_provenance.
- NP781590.RAUQ_ibP-B_oYTEL8GHNArNslU3S0sz_gO9alvS-F2x-E130_assertion wasDerivedFrom befree-20150227 NP781590.RAUQ_ibP-B_oYTEL8GHNArNslU3S0sz_gO9alvS-F2x-E130_provenance.
- NP781590.RAUQ_ibP-B_oYTEL8GHNArNslU3S0sz_gO9alvS-F2x-E130_assertion wasGeneratedBy ECO_0000203 NP781590.RAUQ_ibP-B_oYTEL8GHNArNslU3S0sz_gO9alvS-F2x-E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP781590.RAUQ_ibP-B_oYTEL8GHNArNslU3S0sz_gO9alvS-F2x-E130_provenance.