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- source_evidence_literature type ECO_0000212 NP1307747.RAbIuUFaC_CMVzjsVFKp9gIzSTriu5XdrEsv8iopZ_PVI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1307747.RAbIuUFaC_CMVzjsVFKp9gIzSTriu5XdrEsv8iopZ_PVI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1307747.RAbIuUFaC_CMVzjsVFKp9gIzSTriu5XdrEsv8iopZ_PVI130_provenance.
- NP1307747.RAbIuUFaC_CMVzjsVFKp9gIzSTriu5XdrEsv8iopZ_PVI130_assertion description "[This very low factor IX level and severe bleeding tendency of the patient would be consistent with the homozygous state, but since a double mutation is extremely rare the patient's laboratory findings can be more easily explained by extreme lyonization of the normal X-chromosome of a heterozygous carrier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1307747.RAbIuUFaC_CMVzjsVFKp9gIzSTriu5XdrEsv8iopZ_PVI130_provenance.
- NP1307747.RAbIuUFaC_CMVzjsVFKp9gIzSTriu5XdrEsv8iopZ_PVI130_assertion evidence source_evidence_literature NP1307747.RAbIuUFaC_CMVzjsVFKp9gIzSTriu5XdrEsv8iopZ_PVI130_provenance.
- NP1307747.RAbIuUFaC_CMVzjsVFKp9gIzSTriu5XdrEsv8iopZ_PVI130_assertion SIO_000772 7166026 NP1307747.RAbIuUFaC_CMVzjsVFKp9gIzSTriu5XdrEsv8iopZ_PVI130_provenance.
- NP1307747.RAbIuUFaC_CMVzjsVFKp9gIzSTriu5XdrEsv8iopZ_PVI130_assertion wasDerivedFrom befree-2016 NP1307747.RAbIuUFaC_CMVzjsVFKp9gIzSTriu5XdrEsv8iopZ_PVI130_provenance.
- NP1307747.RAbIuUFaC_CMVzjsVFKp9gIzSTriu5XdrEsv8iopZ_PVI130_assertion wasGeneratedBy ECO_0000203 NP1307747.RAbIuUFaC_CMVzjsVFKp9gIzSTriu5XdrEsv8iopZ_PVI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1307747.RAbIuUFaC_CMVzjsVFKp9gIzSTriu5XdrEsv8iopZ_PVI130_provenance.