Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP244017.RAraSQvh4ObKguqIQ7dcDPiRiSdfYlpL5NQok55NYOHuQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP244017.RAraSQvh4ObKguqIQ7dcDPiRiSdfYlpL5NQok55NYOHuQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP244017.RAraSQvh4ObKguqIQ7dcDPiRiSdfYlpL5NQok55NYOHuQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP244017.RAraSQvh4ObKguqIQ7dcDPiRiSdfYlpL5NQok55NYOHuQ130_provenance.
- NP244017.RAraSQvh4ObKguqIQ7dcDPiRiSdfYlpL5NQok55NYOHuQ130_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." NP244017.RAraSQvh4ObKguqIQ7dcDPiRiSdfYlpL5NQok55NYOHuQ130_provenance.
- NP244017.RAraSQvh4ObKguqIQ7dcDPiRiSdfYlpL5NQok55NYOHuQ130_assertion evidence source_evidence_literature NP244017.RAraSQvh4ObKguqIQ7dcDPiRiSdfYlpL5NQok55NYOHuQ130_provenance.
- NP244017.RAraSQvh4ObKguqIQ7dcDPiRiSdfYlpL5NQok55NYOHuQ130_assertion SIO_000772 10688839 NP244017.RAraSQvh4ObKguqIQ7dcDPiRiSdfYlpL5NQok55NYOHuQ130_provenance.
- NP244017.RAraSQvh4ObKguqIQ7dcDPiRiSdfYlpL5NQok55NYOHuQ130_assertion wasDerivedFrom befree-20140225 NP244017.RAraSQvh4ObKguqIQ7dcDPiRiSdfYlpL5NQok55NYOHuQ130_provenance.
- NP244017.RAraSQvh4ObKguqIQ7dcDPiRiSdfYlpL5NQok55NYOHuQ130_assertion wasGeneratedBy ECO_0000203 NP244017.RAraSQvh4ObKguqIQ7dcDPiRiSdfYlpL5NQok55NYOHuQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP244017.RAraSQvh4ObKguqIQ7dcDPiRiSdfYlpL5NQok55NYOHuQ130_provenance.