Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_assertion> ?p ?o ?g. }
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- NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_assertion type Assertion NP8362.RAT6l1ePKj0FzVnsu85Pavj2uzEmij_ORDBq49otRnr1Y130_head.
- 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.