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- source_evidence_literature type ECO_0000212 NP913108.RAt9_lSEb5GS62gKdl9BLF6cHLeedeFVHKRudJug13wcE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP913108.RAt9_lSEb5GS62gKdl9BLF6cHLeedeFVHKRudJug13wcE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP913108.RAt9_lSEb5GS62gKdl9BLF6cHLeedeFVHKRudJug13wcE130_provenance.
- NP913108.RAt9_lSEb5GS62gKdl9BLF6cHLeedeFVHKRudJug13wcE130_assertion description "[Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP913108.RAt9_lSEb5GS62gKdl9BLF6cHLeedeFVHKRudJug13wcE130_provenance.
- NP913108.RAt9_lSEb5GS62gKdl9BLF6cHLeedeFVHKRudJug13wcE130_assertion evidence source_evidence_literature NP913108.RAt9_lSEb5GS62gKdl9BLF6cHLeedeFVHKRudJug13wcE130_provenance.
- NP913108.RAt9_lSEb5GS62gKdl9BLF6cHLeedeFVHKRudJug13wcE130_assertion SIO_000772 9630669 NP913108.RAt9_lSEb5GS62gKdl9BLF6cHLeedeFVHKRudJug13wcE130_provenance.
- NP913108.RAt9_lSEb5GS62gKdl9BLF6cHLeedeFVHKRudJug13wcE130_assertion wasDerivedFrom befree-20150227 NP913108.RAt9_lSEb5GS62gKdl9BLF6cHLeedeFVHKRudJug13wcE130_provenance.
- NP913108.RAt9_lSEb5GS62gKdl9BLF6cHLeedeFVHKRudJug13wcE130_assertion wasGeneratedBy ECO_0000203 NP913108.RAt9_lSEb5GS62gKdl9BLF6cHLeedeFVHKRudJug13wcE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP913108.RAt9_lSEb5GS62gKdl9BLF6cHLeedeFVHKRudJug13wcE130_provenance.