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- source_evidence_literature type ECO_0000212 NP329818.RAaIJvj89RmnUfEqoF4toEJmW8pmKOyntP4_URL64RuGs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP329818.RAaIJvj89RmnUfEqoF4toEJmW8pmKOyntP4_URL64RuGs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP329818.RAaIJvj89RmnUfEqoF4toEJmW8pmKOyntP4_URL64RuGs130_provenance.
- NP329818.RAaIJvj89RmnUfEqoF4toEJmW8pmKOyntP4_URL64RuGs130_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." NP329818.RAaIJvj89RmnUfEqoF4toEJmW8pmKOyntP4_URL64RuGs130_provenance.
- NP329818.RAaIJvj89RmnUfEqoF4toEJmW8pmKOyntP4_URL64RuGs130_assertion evidence source_evidence_literature NP329818.RAaIJvj89RmnUfEqoF4toEJmW8pmKOyntP4_URL64RuGs130_provenance.
- NP329818.RAaIJvj89RmnUfEqoF4toEJmW8pmKOyntP4_URL64RuGs130_assertion SIO_000772 1829836 NP329818.RAaIJvj89RmnUfEqoF4toEJmW8pmKOyntP4_URL64RuGs130_provenance.
- NP329818.RAaIJvj89RmnUfEqoF4toEJmW8pmKOyntP4_URL64RuGs130_assertion wasDerivedFrom befree-20150227 NP329818.RAaIJvj89RmnUfEqoF4toEJmW8pmKOyntP4_URL64RuGs130_provenance.
- NP329818.RAaIJvj89RmnUfEqoF4toEJmW8pmKOyntP4_URL64RuGs130_assertion wasGeneratedBy ECO_0000203 NP329818.RAaIJvj89RmnUfEqoF4toEJmW8pmKOyntP4_URL64RuGs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP329818.RAaIJvj89RmnUfEqoF4toEJmW8pmKOyntP4_URL64RuGs130_provenance.