Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP600084.RAj4PvAe07O6NIuezANYI2P-XcB1RxQkGZWBl2zjyxxW4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP600084.RAj4PvAe07O6NIuezANYI2P-XcB1RxQkGZWBl2zjyxxW4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP600084.RAj4PvAe07O6NIuezANYI2P-XcB1RxQkGZWBl2zjyxxW4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP600084.RAj4PvAe07O6NIuezANYI2P-XcB1RxQkGZWBl2zjyxxW4130_provenance.
- NP600084.RAj4PvAe07O6NIuezANYI2P-XcB1RxQkGZWBl2zjyxxW4130_assertion description "[The hallmark of the 8p12 stem cell myeloproliferative disorder (MPD) is the disruption of the FGFR1 gene, which encodes a tyrosine kinase receptor for members of the fibroblast growth factor family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600084.RAj4PvAe07O6NIuezANYI2P-XcB1RxQkGZWBl2zjyxxW4130_provenance.
- NP600084.RAj4PvAe07O6NIuezANYI2P-XcB1RxQkGZWBl2zjyxxW4130_assertion evidence source_evidence_literature NP600084.RAj4PvAe07O6NIuezANYI2P-XcB1RxQkGZWBl2zjyxxW4130_provenance.
- NP600084.RAj4PvAe07O6NIuezANYI2P-XcB1RxQkGZWBl2zjyxxW4130_assertion SIO_000772 10688839 NP600084.RAj4PvAe07O6NIuezANYI2P-XcB1RxQkGZWBl2zjyxxW4130_provenance.
- NP600084.RAj4PvAe07O6NIuezANYI2P-XcB1RxQkGZWBl2zjyxxW4130_assertion wasDerivedFrom befree-20150227 NP600084.RAj4PvAe07O6NIuezANYI2P-XcB1RxQkGZWBl2zjyxxW4130_provenance.
- NP600084.RAj4PvAe07O6NIuezANYI2P-XcB1RxQkGZWBl2zjyxxW4130_assertion wasGeneratedBy ECO_0000203 NP600084.RAj4PvAe07O6NIuezANYI2P-XcB1RxQkGZWBl2zjyxxW4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP600084.RAj4PvAe07O6NIuezANYI2P-XcB1RxQkGZWBl2zjyxxW4130_provenance.