Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP192651.RAeYmrI2H1rVgQp1ZD4DJ582ZcCjDLYJerIdk_F587aZ0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP192651.RAeYmrI2H1rVgQp1ZD4DJ582ZcCjDLYJerIdk_F587aZ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP192651.RAeYmrI2H1rVgQp1ZD4DJ582ZcCjDLYJerIdk_F587aZ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP192651.RAeYmrI2H1rVgQp1ZD4DJ582ZcCjDLYJerIdk_F587aZ0130_provenance.
- NP192651.RAeYmrI2H1rVgQp1ZD4DJ582ZcCjDLYJerIdk_F587aZ0130_assertion description "[The C-terminus of the G-CSF receptor, truncated in patients with severe congenital neutropenia/acute myeloid leukemia, is required for SH2-containing phosphatase-1 suppression of G-CSF-stimulated Stat activation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP192651.RAeYmrI2H1rVgQp1ZD4DJ582ZcCjDLYJerIdk_F587aZ0130_provenance.
- NP192651.RAeYmrI2H1rVgQp1ZD4DJ582ZcCjDLYJerIdk_F587aZ0130_assertion evidence source_evidence_literature NP192651.RAeYmrI2H1rVgQp1ZD4DJ582ZcCjDLYJerIdk_F587aZ0130_provenance.
- NP192651.RAeYmrI2H1rVgQp1ZD4DJ582ZcCjDLYJerIdk_F587aZ0130_assertion SIO_000772 11714811 NP192651.RAeYmrI2H1rVgQp1ZD4DJ582ZcCjDLYJerIdk_F587aZ0130_provenance.
- NP192651.RAeYmrI2H1rVgQp1ZD4DJ582ZcCjDLYJerIdk_F587aZ0130_assertion wasDerivedFrom lhgdn-20090331 NP192651.RAeYmrI2H1rVgQp1ZD4DJ582ZcCjDLYJerIdk_F587aZ0130_provenance.
- NP192651.RAeYmrI2H1rVgQp1ZD4DJ582ZcCjDLYJerIdk_F587aZ0130_assertion wasGeneratedBy ECO_0000203 NP192651.RAeYmrI2H1rVgQp1ZD4DJ582ZcCjDLYJerIdk_F587aZ0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP192651.RAeYmrI2H1rVgQp1ZD4DJ582ZcCjDLYJerIdk_F587aZ0130_provenance.