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- source_evidence_literature type ECO_0000212 NP1247422.RAKWDc9uCHgO9JzwHK5qzanK0-Zej9KIU9AcM5AACDnmU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1247422.RAKWDc9uCHgO9JzwHK5qzanK0-Zej9KIU9AcM5AACDnmU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1247422.RAKWDc9uCHgO9JzwHK5qzanK0-Zej9KIU9AcM5AACDnmU130_provenance.
- NP1247422.RAKWDc9uCHgO9JzwHK5qzanK0-Zej9KIU9AcM5AACDnmU130_assertion description "[Thus, clinical and experimental analyses have identified novel AR-signalling defects associated with mutations in the structurally disordered AR-NTD domain in patients with AIS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247422.RAKWDc9uCHgO9JzwHK5qzanK0-Zej9KIU9AcM5AACDnmU130_provenance.
- NP1247422.RAKWDc9uCHgO9JzwHK5qzanK0-Zej9KIU9AcM5AACDnmU130_assertion evidence source_evidence_literature NP1247422.RAKWDc9uCHgO9JzwHK5qzanK0-Zej9KIU9AcM5AACDnmU130_provenance.
- NP1247422.RAKWDc9uCHgO9JzwHK5qzanK0-Zej9KIU9AcM5AACDnmU130_assertion SIO_000772 25500996 NP1247422.RAKWDc9uCHgO9JzwHK5qzanK0-Zej9KIU9AcM5AACDnmU130_provenance.
- NP1247422.RAKWDc9uCHgO9JzwHK5qzanK0-Zej9KIU9AcM5AACDnmU130_assertion wasDerivedFrom befree-2016 NP1247422.RAKWDc9uCHgO9JzwHK5qzanK0-Zej9KIU9AcM5AACDnmU130_provenance.
- NP1247422.RAKWDc9uCHgO9JzwHK5qzanK0-Zej9KIU9AcM5AACDnmU130_assertion wasGeneratedBy ECO_0000203 NP1247422.RAKWDc9uCHgO9JzwHK5qzanK0-Zej9KIU9AcM5AACDnmU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1247422.RAKWDc9uCHgO9JzwHK5qzanK0-Zej9KIU9AcM5AACDnmU130_provenance.