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- source_evidence_literature type ECO_0000212 NP856994.RA-3dxJgKLI-DeHRG8zaFnbPwDcBiSbNwWIkHzb_Ow8DY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP856994.RA-3dxJgKLI-DeHRG8zaFnbPwDcBiSbNwWIkHzb_Ow8DY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP856994.RA-3dxJgKLI-DeHRG8zaFnbPwDcBiSbNwWIkHzb_Ow8DY130_provenance.
- NP856994.RA-3dxJgKLI-DeHRG8zaFnbPwDcBiSbNwWIkHzb_Ow8DY130_assertion description "[Furthermore, we discovered mutations in both alleles of POLR1C in three individuals with TCS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856994.RA-3dxJgKLI-DeHRG8zaFnbPwDcBiSbNwWIkHzb_Ow8DY130_provenance.
- NP856994.RA-3dxJgKLI-DeHRG8zaFnbPwDcBiSbNwWIkHzb_Ow8DY130_assertion evidence source_evidence_literature NP856994.RA-3dxJgKLI-DeHRG8zaFnbPwDcBiSbNwWIkHzb_Ow8DY130_provenance.
- NP856994.RA-3dxJgKLI-DeHRG8zaFnbPwDcBiSbNwWIkHzb_Ow8DY130_assertion SIO_000772 21131976 NP856994.RA-3dxJgKLI-DeHRG8zaFnbPwDcBiSbNwWIkHzb_Ow8DY130_provenance.
- NP856994.RA-3dxJgKLI-DeHRG8zaFnbPwDcBiSbNwWIkHzb_Ow8DY130_assertion wasDerivedFrom befree-2016 NP856994.RA-3dxJgKLI-DeHRG8zaFnbPwDcBiSbNwWIkHzb_Ow8DY130_provenance.
- NP856994.RA-3dxJgKLI-DeHRG8zaFnbPwDcBiSbNwWIkHzb_Ow8DY130_assertion wasGeneratedBy ECO_0000203 NP856994.RA-3dxJgKLI-DeHRG8zaFnbPwDcBiSbNwWIkHzb_Ow8DY130_provenance.
- befree-2016 importedOn "2016-02-19" NP856994.RA-3dxJgKLI-DeHRG8zaFnbPwDcBiSbNwWIkHzb_Ow8DY130_provenance.