Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP8641.RAQ__Hnzvp-rdGXGvomvYmhc29gbu_xXoSa6SDfcNbN2Y130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP8641.RAQ__Hnzvp-rdGXGvomvYmhc29gbu_xXoSa6SDfcNbN2Y130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8641.RAQ__Hnzvp-rdGXGvomvYmhc29gbu_xXoSa6SDfcNbN2Y130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8641.RAQ__Hnzvp-rdGXGvomvYmhc29gbu_xXoSa6SDfcNbN2Y130_provenance.
- NP8641.RAQ__Hnzvp-rdGXGvomvYmhc29gbu_xXoSa6SDfcNbN2Y130_assertion description "[This mutation caused the mildest form of all androgen insensitivity syndromes ever examined for mutations in the androgen receptor gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8641.RAQ__Hnzvp-rdGXGvomvYmhc29gbu_xXoSa6SDfcNbN2Y130_provenance.
- NP8641.RAQ__Hnzvp-rdGXGvomvYmhc29gbu_xXoSa6SDfcNbN2Y130_assertion evidence source_evidence_curated NP8641.RAQ__Hnzvp-rdGXGvomvYmhc29gbu_xXoSa6SDfcNbN2Y130_provenance.
- NP8641.RAQ__Hnzvp-rdGXGvomvYmhc29gbu_xXoSa6SDfcNbN2Y130_assertion SIO_000772 7962294 NP8641.RAQ__Hnzvp-rdGXGvomvYmhc29gbu_xXoSa6SDfcNbN2Y130_provenance.
- NP8641.RAQ__Hnzvp-rdGXGvomvYmhc29gbu_xXoSa6SDfcNbN2Y130_assertion wasDerivedFrom uniprot-2016 NP8641.RAQ__Hnzvp-rdGXGvomvYmhc29gbu_xXoSa6SDfcNbN2Y130_provenance.
- NP8641.RAQ__Hnzvp-rdGXGvomvYmhc29gbu_xXoSa6SDfcNbN2Y130_assertion wasGeneratedBy ECO_0000218 NP8641.RAQ__Hnzvp-rdGXGvomvYmhc29gbu_xXoSa6SDfcNbN2Y130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP8641.RAQ__Hnzvp-rdGXGvomvYmhc29gbu_xXoSa6SDfcNbN2Y130_provenance.