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- source_evidence_literature type ECO_0000212 NP1153244.RAH32h1Y-a1eCYZbKsvJBim42m_8A49sEmPpsA6NHlTYU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1153244.RAH32h1Y-a1eCYZbKsvJBim42m_8A49sEmPpsA6NHlTYU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1153244.RAH32h1Y-a1eCYZbKsvJBim42m_8A49sEmPpsA6NHlTYU130_provenance.
- NP1153244.RAH32h1Y-a1eCYZbKsvJBim42m_8A49sEmPpsA6NHlTYU130_assertion description "[In up to 70% of patients with MDS clonal chromosome abnormalities can be identified which have a high impact on setting the correct diagnosis and estimation of prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1153244.RAH32h1Y-a1eCYZbKsvJBim42m_8A49sEmPpsA6NHlTYU130_provenance.
- NP1153244.RAH32h1Y-a1eCYZbKsvJBim42m_8A49sEmPpsA6NHlTYU130_assertion evidence source_evidence_literature NP1153244.RAH32h1Y-a1eCYZbKsvJBim42m_8A49sEmPpsA6NHlTYU130_provenance.
- NP1153244.RAH32h1Y-a1eCYZbKsvJBim42m_8A49sEmPpsA6NHlTYU130_assertion SIO_000772 24507811 NP1153244.RAH32h1Y-a1eCYZbKsvJBim42m_8A49sEmPpsA6NHlTYU130_provenance.
- NP1153244.RAH32h1Y-a1eCYZbKsvJBim42m_8A49sEmPpsA6NHlTYU130_assertion wasDerivedFrom befree-2016 NP1153244.RAH32h1Y-a1eCYZbKsvJBim42m_8A49sEmPpsA6NHlTYU130_provenance.
- NP1153244.RAH32h1Y-a1eCYZbKsvJBim42m_8A49sEmPpsA6NHlTYU130_assertion wasGeneratedBy ECO_0000203 NP1153244.RAH32h1Y-a1eCYZbKsvJBim42m_8A49sEmPpsA6NHlTYU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1153244.RAH32h1Y-a1eCYZbKsvJBim42m_8A49sEmPpsA6NHlTYU130_provenance.