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- source_evidence_literature type ECO_0000212 NP294762.RA0TW1R6LFZcQ70TFrW3Fkij90mLo8SdvRE_XV-24VQC4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294762.RA0TW1R6LFZcQ70TFrW3Fkij90mLo8SdvRE_XV-24VQC4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294762.RA0TW1R6LFZcQ70TFrW3Fkij90mLo8SdvRE_XV-24VQC4130_provenance.
- NP294762.RA0TW1R6LFZcQ70TFrW3Fkij90mLo8SdvRE_XV-24VQC4130_assertion description "[We have mapped this gene to the 3 Mb critical region of gene loss of the 5q- syndrome within 5q32, flanked by the genes for ADRB2 and IL12B, using gene dosage analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294762.RA0TW1R6LFZcQ70TFrW3Fkij90mLo8SdvRE_XV-24VQC4130_provenance.
- NP294762.RA0TW1R6LFZcQ70TFrW3Fkij90mLo8SdvRE_XV-24VQC4130_assertion evidence source_evidence_literature NP294762.RA0TW1R6LFZcQ70TFrW3Fkij90mLo8SdvRE_XV-24VQC4130_provenance.
- NP294762.RA0TW1R6LFZcQ70TFrW3Fkij90mLo8SdvRE_XV-24VQC4130_assertion SIO_000772 10982193 NP294762.RA0TW1R6LFZcQ70TFrW3Fkij90mLo8SdvRE_XV-24VQC4130_provenance.
- NP294762.RA0TW1R6LFZcQ70TFrW3Fkij90mLo8SdvRE_XV-24VQC4130_assertion wasDerivedFrom befree-2016 NP294762.RA0TW1R6LFZcQ70TFrW3Fkij90mLo8SdvRE_XV-24VQC4130_provenance.
- NP294762.RA0TW1R6LFZcQ70TFrW3Fkij90mLo8SdvRE_XV-24VQC4130_assertion wasGeneratedBy ECO_0000203 NP294762.RA0TW1R6LFZcQ70TFrW3Fkij90mLo8SdvRE_XV-24VQC4130_provenance.
- befree-2016 importedOn "2016-02-19" NP294762.RA0TW1R6LFZcQ70TFrW3Fkij90mLo8SdvRE_XV-24VQC4130_provenance.