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- source_evidence_literature type ECO_0000212 NP867541.RASRosohBViHYvtQH21_0_ALrawQ08eYR-YuMzt1fnsbc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867541.RASRosohBViHYvtQH21_0_ALrawQ08eYR-YuMzt1fnsbc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867541.RASRosohBViHYvtQH21_0_ALrawQ08eYR-YuMzt1fnsbc130_provenance.
- NP867541.RASRosohBViHYvtQH21_0_ALrawQ08eYR-YuMzt1fnsbc130_assertion description "[When the results of the FGFR3 thanatophoric dysplasia mutations located in exon 7, A248C and S249C and in exon 10, G372C and T375C, were analyzed one by one or as a group, despite the findings of previous research reports, our data suggest that these mutations are detected homogenously regardless of the tumor classification and tumor grade.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867541.RASRosohBViHYvtQH21_0_ALrawQ08eYR-YuMzt1fnsbc130_provenance.
- NP867541.RASRosohBViHYvtQH21_0_ALrawQ08eYR-YuMzt1fnsbc130_assertion evidence source_evidence_literature NP867541.RASRosohBViHYvtQH21_0_ALrawQ08eYR-YuMzt1fnsbc130_provenance.
- NP867541.RASRosohBViHYvtQH21_0_ALrawQ08eYR-YuMzt1fnsbc130_assertion SIO_000772 21264819 NP867541.RASRosohBViHYvtQH21_0_ALrawQ08eYR-YuMzt1fnsbc130_provenance.
- NP867541.RASRosohBViHYvtQH21_0_ALrawQ08eYR-YuMzt1fnsbc130_assertion wasDerivedFrom befree-2016 NP867541.RASRosohBViHYvtQH21_0_ALrawQ08eYR-YuMzt1fnsbc130_provenance.
- NP867541.RASRosohBViHYvtQH21_0_ALrawQ08eYR-YuMzt1fnsbc130_assertion wasGeneratedBy ECO_0000203 NP867541.RASRosohBViHYvtQH21_0_ALrawQ08eYR-YuMzt1fnsbc130_provenance.
- befree-2016 importedOn "2016-02-19" NP867541.RASRosohBViHYvtQH21_0_ALrawQ08eYR-YuMzt1fnsbc130_provenance.