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- source_evidence_literature type ECO_0000212 NP825886.RA9pHSVDKVBiubQO2J7mTRDxS3den7_g-Jb2EqSXwhxUE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP825886.RA9pHSVDKVBiubQO2J7mTRDxS3den7_g-Jb2EqSXwhxUE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP825886.RA9pHSVDKVBiubQO2J7mTRDxS3den7_g-Jb2EqSXwhxUE130_provenance.
- NP825886.RA9pHSVDKVBiubQO2J7mTRDxS3den7_g-Jb2EqSXwhxUE130_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." NP825886.RA9pHSVDKVBiubQO2J7mTRDxS3den7_g-Jb2EqSXwhxUE130_provenance.
- NP825886.RA9pHSVDKVBiubQO2J7mTRDxS3den7_g-Jb2EqSXwhxUE130_assertion evidence source_evidence_literature NP825886.RA9pHSVDKVBiubQO2J7mTRDxS3den7_g-Jb2EqSXwhxUE130_provenance.
- NP825886.RA9pHSVDKVBiubQO2J7mTRDxS3den7_g-Jb2EqSXwhxUE130_assertion SIO_000772 21131976 NP825886.RA9pHSVDKVBiubQO2J7mTRDxS3den7_g-Jb2EqSXwhxUE130_provenance.
- NP825886.RA9pHSVDKVBiubQO2J7mTRDxS3den7_g-Jb2EqSXwhxUE130_assertion wasDerivedFrom befree-20150227 NP825886.RA9pHSVDKVBiubQO2J7mTRDxS3den7_g-Jb2EqSXwhxUE130_provenance.
- NP825886.RA9pHSVDKVBiubQO2J7mTRDxS3den7_g-Jb2EqSXwhxUE130_assertion wasGeneratedBy ECO_0000203 NP825886.RA9pHSVDKVBiubQO2J7mTRDxS3den7_g-Jb2EqSXwhxUE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP825886.RA9pHSVDKVBiubQO2J7mTRDxS3den7_g-Jb2EqSXwhxUE130_provenance.