Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_provenance.
- NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_assertion description "[In summary, missense mutations within the exons of the androgen receptor gene encoding the steroid-binding domain of the receptor are common causes of both partial and complete forms of androgen insensitivity syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_provenance.
- NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_assertion evidence source_evidence_curated NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_provenance.
- NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_assertion SIO_000772 7581399 NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_provenance.
- NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_assertion wasDerivedFrom uniprot-2016 NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_provenance.
- NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_assertion wasGeneratedBy ECO_0000218 NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_provenance.