Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1053369.RAAi6W5nITYrEHQXvDlZi9APj0keQj1N66rVgvfvnTOtQ130_assertion> ?p ?o ?g. }
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- NP1053369.RAAi6W5nITYrEHQXvDlZi9APj0keQj1N66rVgvfvnTOtQ130_assertion type Assertion NP1053369.RAAi6W5nITYrEHQXvDlZi9APj0keQj1N66rVgvfvnTOtQ130_head.
- NP1053369.RAAi6W5nITYrEHQXvDlZi9APj0keQj1N66rVgvfvnTOtQ130_assertion description "[The complete form of androgen insensitivity is an inherited X-linked syndrome in which genetic males fail to undergo masculinization in utero due to defective functioning of the androgen receptor (AR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1053369.RAAi6W5nITYrEHQXvDlZi9APj0keQj1N66rVgvfvnTOtQ130_provenance.
- NP1053369.RAAi6W5nITYrEHQXvDlZi9APj0keQj1N66rVgvfvnTOtQ130_assertion evidence source_evidence_literature NP1053369.RAAi6W5nITYrEHQXvDlZi9APj0keQj1N66rVgvfvnTOtQ130_provenance.
- NP1053369.RAAi6W5nITYrEHQXvDlZi9APj0keQj1N66rVgvfvnTOtQ130_assertion SIO_000772 2341409 NP1053369.RAAi6W5nITYrEHQXvDlZi9APj0keQj1N66rVgvfvnTOtQ130_provenance.
- NP1053369.RAAi6W5nITYrEHQXvDlZi9APj0keQj1N66rVgvfvnTOtQ130_assertion wasDerivedFrom befree-2016 NP1053369.RAAi6W5nITYrEHQXvDlZi9APj0keQj1N66rVgvfvnTOtQ130_provenance.
- NP1053369.RAAi6W5nITYrEHQXvDlZi9APj0keQj1N66rVgvfvnTOtQ130_assertion wasGeneratedBy ECO_0000203 NP1053369.RAAi6W5nITYrEHQXvDlZi9APj0keQj1N66rVgvfvnTOtQ130_provenance.