Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP401.RAYRSzUsor3XqRgPi6KDkCiR3X-PR74sxGNq51UeUD_RQ130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP401.RAYRSzUsor3XqRgPi6KDkCiR3X-PR74sxGNq51UeUD_RQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP401.RAYRSzUsor3XqRgPi6KDkCiR3X-PR74sxGNq51UeUD_RQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP401.RAYRSzUsor3XqRgPi6KDkCiR3X-PR74sxGNq51UeUD_RQ130_provenance.
- NP401.RAYRSzUsor3XqRgPi6KDkCiR3X-PR74sxGNq51UeUD_RQ130_assertion description "[A novel point mutation (R840S) in the androgen receptor in a Brazilian family with partial androgen insensitivity syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401.RAYRSzUsor3XqRgPi6KDkCiR3X-PR74sxGNq51UeUD_RQ130_provenance.
- NP401.RAYRSzUsor3XqRgPi6KDkCiR3X-PR74sxGNq51UeUD_RQ130_assertion evidence source_evidence_curated NP401.RAYRSzUsor3XqRgPi6KDkCiR3X-PR74sxGNq51UeUD_RQ130_provenance.
- NP401.RAYRSzUsor3XqRgPi6KDkCiR3X-PR74sxGNq51UeUD_RQ130_assertion SIO_000772 10502786 NP401.RAYRSzUsor3XqRgPi6KDkCiR3X-PR74sxGNq51UeUD_RQ130_provenance.
- NP401.RAYRSzUsor3XqRgPi6KDkCiR3X-PR74sxGNq51UeUD_RQ130_assertion wasDerivedFrom uniprot-2016 NP401.RAYRSzUsor3XqRgPi6KDkCiR3X-PR74sxGNq51UeUD_RQ130_provenance.
- NP401.RAYRSzUsor3XqRgPi6KDkCiR3X-PR74sxGNq51UeUD_RQ130_assertion wasGeneratedBy ECO_0000218 NP401.RAYRSzUsor3XqRgPi6KDkCiR3X-PR74sxGNq51UeUD_RQ130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP401.RAYRSzUsor3XqRgPi6KDkCiR3X-PR74sxGNq51UeUD_RQ130_provenance.