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- source_evidence_literature type ECO_0000212 NP712212.RANElT80UqHCYy_GnhAntqE2D6PZTIirIAUqq1mXCF_TM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP712212.RANElT80UqHCYy_GnhAntqE2D6PZTIirIAUqq1mXCF_TM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP712212.RANElT80UqHCYy_GnhAntqE2D6PZTIirIAUqq1mXCF_TM130_provenance.
- NP712212.RANElT80UqHCYy_GnhAntqE2D6PZTIirIAUqq1mXCF_TM130_assertion description "[Molecular analysis of the 5 alpha-reductase type 2 gene in a patient with confirmed biochemical 5 alpha-reductase deficiency has resulted in the identification of a novel mutation, GAA to AAA, at codon 200.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP712212.RANElT80UqHCYy_GnhAntqE2D6PZTIirIAUqq1mXCF_TM130_provenance.
- NP712212.RANElT80UqHCYy_GnhAntqE2D6PZTIirIAUqq1mXCF_TM130_assertion evidence source_evidence_literature NP712212.RANElT80UqHCYy_GnhAntqE2D6PZTIirIAUqq1mXCF_TM130_provenance.
- NP712212.RANElT80UqHCYy_GnhAntqE2D6PZTIirIAUqq1mXCF_TM130_assertion SIO_000772 9208814 NP712212.RANElT80UqHCYy_GnhAntqE2D6PZTIirIAUqq1mXCF_TM130_provenance.
- NP712212.RANElT80UqHCYy_GnhAntqE2D6PZTIirIAUqq1mXCF_TM130_assertion wasDerivedFrom befree-20150227 NP712212.RANElT80UqHCYy_GnhAntqE2D6PZTIirIAUqq1mXCF_TM130_provenance.
- NP712212.RANElT80UqHCYy_GnhAntqE2D6PZTIirIAUqq1mXCF_TM130_assertion wasGeneratedBy ECO_0000203 NP712212.RANElT80UqHCYy_GnhAntqE2D6PZTIirIAUqq1mXCF_TM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP712212.RANElT80UqHCYy_GnhAntqE2D6PZTIirIAUqq1mXCF_TM130_provenance.