Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP303478.RA9ItnOPXSygDhHchGAVjjSh_bbFi86COR4kj3gY7Q86I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP303478.RA9ItnOPXSygDhHchGAVjjSh_bbFi86COR4kj3gY7Q86I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP303478.RA9ItnOPXSygDhHchGAVjjSh_bbFi86COR4kj3gY7Q86I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP303478.RA9ItnOPXSygDhHchGAVjjSh_bbFi86COR4kj3gY7Q86I130_provenance.
- NP303478.RA9ItnOPXSygDhHchGAVjjSh_bbFi86COR4kj3gY7Q86I130_assertion description "[Point mutations in the G-CSF receptor gene are found in about 20% of SCN patients who are predisposed to MDS/AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP303478.RA9ItnOPXSygDhHchGAVjjSh_bbFi86COR4kj3gY7Q86I130_provenance.
- NP303478.RA9ItnOPXSygDhHchGAVjjSh_bbFi86COR4kj3gY7Q86I130_assertion evidence source_evidence_literature NP303478.RA9ItnOPXSygDhHchGAVjjSh_bbFi86COR4kj3gY7Q86I130_provenance.
- NP303478.RA9ItnOPXSygDhHchGAVjjSh_bbFi86COR4kj3gY7Q86I130_assertion SIO_000772 11122117 NP303478.RA9ItnOPXSygDhHchGAVjjSh_bbFi86COR4kj3gY7Q86I130_provenance.
- NP303478.RA9ItnOPXSygDhHchGAVjjSh_bbFi86COR4kj3gY7Q86I130_assertion wasDerivedFrom befree-2016 NP303478.RA9ItnOPXSygDhHchGAVjjSh_bbFi86COR4kj3gY7Q86I130_provenance.
- NP303478.RA9ItnOPXSygDhHchGAVjjSh_bbFi86COR4kj3gY7Q86I130_assertion wasGeneratedBy ECO_0000203 NP303478.RA9ItnOPXSygDhHchGAVjjSh_bbFi86COR4kj3gY7Q86I130_provenance.
- befree-2016 importedOn "2016-02-19" NP303478.RA9ItnOPXSygDhHchGAVjjSh_bbFi86COR4kj3gY7Q86I130_provenance.