Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1247423.RA3T8mvaK6jWo3rsYIV5A7WOhZpYMRm0C30PQJyh9Ht-8130_assertion> ?p ?o ?g. }
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- NP1247423.RA3T8mvaK6jWo3rsYIV5A7WOhZpYMRm0C30PQJyh9Ht-8130_assertion type Assertion NP1247423.RA3T8mvaK6jWo3rsYIV5A7WOhZpYMRm0C30PQJyh9Ht-8130_head.
- NP1247423.RA3T8mvaK6jWo3rsYIV5A7WOhZpYMRm0C30PQJyh9Ht-8130_assertion description "[Thus, clinical and experimental analyses have identified novel AR-signalling defects associated with mutations in the structurally disordered AR-NTD domain in patients with AIS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247423.RA3T8mvaK6jWo3rsYIV5A7WOhZpYMRm0C30PQJyh9Ht-8130_provenance.
- NP1247423.RA3T8mvaK6jWo3rsYIV5A7WOhZpYMRm0C30PQJyh9Ht-8130_assertion evidence source_evidence_literature NP1247423.RA3T8mvaK6jWo3rsYIV5A7WOhZpYMRm0C30PQJyh9Ht-8130_provenance.
- NP1247423.RA3T8mvaK6jWo3rsYIV5A7WOhZpYMRm0C30PQJyh9Ht-8130_assertion SIO_000772 25500996 NP1247423.RA3T8mvaK6jWo3rsYIV5A7WOhZpYMRm0C30PQJyh9Ht-8130_provenance.
- NP1247423.RA3T8mvaK6jWo3rsYIV5A7WOhZpYMRm0C30PQJyh9Ht-8130_assertion wasDerivedFrom befree-2016 NP1247423.RA3T8mvaK6jWo3rsYIV5A7WOhZpYMRm0C30PQJyh9Ht-8130_provenance.
- NP1247423.RA3T8mvaK6jWo3rsYIV5A7WOhZpYMRm0C30PQJyh9Ht-8130_assertion wasGeneratedBy ECO_0000203 NP1247423.RA3T8mvaK6jWo3rsYIV5A7WOhZpYMRm0C30PQJyh9Ht-8130_provenance.