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- source_evidence_literature type ECO_0000212 NP276063.RAVj0S4-PL_1Kce4lPHQX8aJrvTNeWXsnT8iS5C6PY9b4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP276063.RAVj0S4-PL_1Kce4lPHQX8aJrvTNeWXsnT8iS5C6PY9b4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP276063.RAVj0S4-PL_1Kce4lPHQX8aJrvTNeWXsnT8iS5C6PY9b4130_provenance.
- NP276063.RAVj0S4-PL_1Kce4lPHQX8aJrvTNeWXsnT8iS5C6PY9b4130_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." NP276063.RAVj0S4-PL_1Kce4lPHQX8aJrvTNeWXsnT8iS5C6PY9b4130_provenance.
- NP276063.RAVj0S4-PL_1Kce4lPHQX8aJrvTNeWXsnT8iS5C6PY9b4130_assertion evidence source_evidence_literature NP276063.RAVj0S4-PL_1Kce4lPHQX8aJrvTNeWXsnT8iS5C6PY9b4130_provenance.
- NP276063.RAVj0S4-PL_1Kce4lPHQX8aJrvTNeWXsnT8iS5C6PY9b4130_assertion SIO_000772 10688839 NP276063.RAVj0S4-PL_1Kce4lPHQX8aJrvTNeWXsnT8iS5C6PY9b4130_provenance.
- NP276063.RAVj0S4-PL_1Kce4lPHQX8aJrvTNeWXsnT8iS5C6PY9b4130_assertion wasDerivedFrom befree-2016 NP276063.RAVj0S4-PL_1Kce4lPHQX8aJrvTNeWXsnT8iS5C6PY9b4130_provenance.
- NP276063.RAVj0S4-PL_1Kce4lPHQX8aJrvTNeWXsnT8iS5C6PY9b4130_assertion wasGeneratedBy ECO_0000203 NP276063.RAVj0S4-PL_1Kce4lPHQX8aJrvTNeWXsnT8iS5C6PY9b4130_provenance.
- befree-2016 importedOn "2016-02-19" NP276063.RAVj0S4-PL_1Kce4lPHQX8aJrvTNeWXsnT8iS5C6PY9b4130_provenance.