Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1318654.RAkN5Vs1SAgUCzmgwcYSDZmq1wBqrRnwYxzhGhb8YxFCY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1318654.RAkN5Vs1SAgUCzmgwcYSDZmq1wBqrRnwYxzhGhb8YxFCY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1318654.RAkN5Vs1SAgUCzmgwcYSDZmq1wBqrRnwYxzhGhb8YxFCY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1318654.RAkN5Vs1SAgUCzmgwcYSDZmq1wBqrRnwYxzhGhb8YxFCY130_provenance.
- NP1318654.RAkN5Vs1SAgUCzmgwcYSDZmq1wBqrRnwYxzhGhb8YxFCY130_assertion description "[These exons include positions analogous to those mutated in the FMS gene (colony-stimulating factor-1 receptor) in myelodysplastic syndrome (MDS) and mutated/deleted in the Dominant White Spotting mouse (W locus) which results in macrocytic anaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1318654.RAkN5Vs1SAgUCzmgwcYSDZmq1wBqrRnwYxzhGhb8YxFCY130_provenance.
- NP1318654.RAkN5Vs1SAgUCzmgwcYSDZmq1wBqrRnwYxzhGhb8YxFCY130_assertion evidence source_evidence_literature NP1318654.RAkN5Vs1SAgUCzmgwcYSDZmq1wBqrRnwYxzhGhb8YxFCY130_provenance.
- NP1318654.RAkN5Vs1SAgUCzmgwcYSDZmq1wBqrRnwYxzhGhb8YxFCY130_assertion SIO_000772 7694008 NP1318654.RAkN5Vs1SAgUCzmgwcYSDZmq1wBqrRnwYxzhGhb8YxFCY130_provenance.
- NP1318654.RAkN5Vs1SAgUCzmgwcYSDZmq1wBqrRnwYxzhGhb8YxFCY130_assertion wasDerivedFrom befree-2016 NP1318654.RAkN5Vs1SAgUCzmgwcYSDZmq1wBqrRnwYxzhGhb8YxFCY130_provenance.
- NP1318654.RAkN5Vs1SAgUCzmgwcYSDZmq1wBqrRnwYxzhGhb8YxFCY130_assertion wasGeneratedBy ECO_0000203 NP1318654.RAkN5Vs1SAgUCzmgwcYSDZmq1wBqrRnwYxzhGhb8YxFCY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1318654.RAkN5Vs1SAgUCzmgwcYSDZmq1wBqrRnwYxzhGhb8YxFCY130_provenance.