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- source_evidence_literature type ECO_0000212 NP977301.RAIrij5GcgBuDqe-EgTyAgCqpeN-IBmIMfF4bM6YvdjGY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977301.RAIrij5GcgBuDqe-EgTyAgCqpeN-IBmIMfF4bM6YvdjGY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977301.RAIrij5GcgBuDqe-EgTyAgCqpeN-IBmIMfF4bM6YvdjGY130_provenance.
- NP977301.RAIrij5GcgBuDqe-EgTyAgCqpeN-IBmIMfF4bM6YvdjGY130_assertion description "[In a second cross-sectional study, 1318 unrelated anonymous samples collected in 2003-2007 from patients with a broad range of signs typically found in neurofibromatosis type 1 (NF1) but no detectable NF1 germline mutation underwent SPRED1 mutation analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977301.RAIrij5GcgBuDqe-EgTyAgCqpeN-IBmIMfF4bM6YvdjGY130_provenance.
- NP977301.RAIrij5GcgBuDqe-EgTyAgCqpeN-IBmIMfF4bM6YvdjGY130_assertion evidence source_evidence_literature NP977301.RAIrij5GcgBuDqe-EgTyAgCqpeN-IBmIMfF4bM6YvdjGY130_provenance.
- NP977301.RAIrij5GcgBuDqe-EgTyAgCqpeN-IBmIMfF4bM6YvdjGY130_assertion SIO_000772 19920235 NP977301.RAIrij5GcgBuDqe-EgTyAgCqpeN-IBmIMfF4bM6YvdjGY130_provenance.
- NP977301.RAIrij5GcgBuDqe-EgTyAgCqpeN-IBmIMfF4bM6YvdjGY130_assertion wasDerivedFrom befree-20150227 NP977301.RAIrij5GcgBuDqe-EgTyAgCqpeN-IBmIMfF4bM6YvdjGY130_provenance.
- NP977301.RAIrij5GcgBuDqe-EgTyAgCqpeN-IBmIMfF4bM6YvdjGY130_assertion wasGeneratedBy ECO_0000203 NP977301.RAIrij5GcgBuDqe-EgTyAgCqpeN-IBmIMfF4bM6YvdjGY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP977301.RAIrij5GcgBuDqe-EgTyAgCqpeN-IBmIMfF4bM6YvdjGY130_provenance.