Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP908033.RAR_tUpS2hLfPGYX91qxCir-FobnwHQvpgXm89n8FX14s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP908033.RAR_tUpS2hLfPGYX91qxCir-FobnwHQvpgXm89n8FX14s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP908033.RAR_tUpS2hLfPGYX91qxCir-FobnwHQvpgXm89n8FX14s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP908033.RAR_tUpS2hLfPGYX91qxCir-FobnwHQvpgXm89n8FX14s130_provenance.
- NP908033.RAR_tUpS2hLfPGYX91qxCir-FobnwHQvpgXm89n8FX14s130_assertion description "[Here, we report somatic inactivating mutations and deletion of the X-linked FOXP3 gene residing at Xp11.23 in human prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908033.RAR_tUpS2hLfPGYX91qxCir-FobnwHQvpgXm89n8FX14s130_provenance.
- NP908033.RAR_tUpS2hLfPGYX91qxCir-FobnwHQvpgXm89n8FX14s130_assertion evidence source_evidence_literature NP908033.RAR_tUpS2hLfPGYX91qxCir-FobnwHQvpgXm89n8FX14s130_provenance.
- NP908033.RAR_tUpS2hLfPGYX91qxCir-FobnwHQvpgXm89n8FX14s130_assertion SIO_000772 19800578 NP908033.RAR_tUpS2hLfPGYX91qxCir-FobnwHQvpgXm89n8FX14s130_provenance.
- NP908033.RAR_tUpS2hLfPGYX91qxCir-FobnwHQvpgXm89n8FX14s130_assertion wasDerivedFrom befree-20140225 NP908033.RAR_tUpS2hLfPGYX91qxCir-FobnwHQvpgXm89n8FX14s130_provenance.
- NP908033.RAR_tUpS2hLfPGYX91qxCir-FobnwHQvpgXm89n8FX14s130_assertion wasGeneratedBy ECO_0000203 NP908033.RAR_tUpS2hLfPGYX91qxCir-FobnwHQvpgXm89n8FX14s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP908033.RAR_tUpS2hLfPGYX91qxCir-FobnwHQvpgXm89n8FX14s130_provenance.