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- NP626323.RAtIipHOWS5ItinuEdtcoYkQG7gVijDTj8rL0x0_V08CI130_assertion type Assertion NP626323.RAtIipHOWS5ItinuEdtcoYkQG7gVijDTj8rL0x0_V08CI130_head.
- NP626323.RAtIipHOWS5ItinuEdtcoYkQG7gVijDTj8rL0x0_V08CI130_assertion wasGeneratedBy ECO_0000203 NP626323.RAtIipHOWS5ItinuEdtcoYkQG7gVijDTj8rL0x0_V08CI130_provenance.
- NP626323.RAtIipHOWS5ItinuEdtcoYkQG7gVijDTj8rL0x0_V08CI130_assertion wasDerivedFrom befree-2016 NP626323.RAtIipHOWS5ItinuEdtcoYkQG7gVijDTj8rL0x0_V08CI130_provenance.
- NP626323.RAtIipHOWS5ItinuEdtcoYkQG7gVijDTj8rL0x0_V08CI130_assertion SIO_000772 17714709 NP626323.RAtIipHOWS5ItinuEdtcoYkQG7gVijDTj8rL0x0_V08CI130_provenance.
- NP626323.RAtIipHOWS5ItinuEdtcoYkQG7gVijDTj8rL0x0_V08CI130_assertion evidence source_evidence_literature NP626323.RAtIipHOWS5ItinuEdtcoYkQG7gVijDTj8rL0x0_V08CI130_provenance.
- NP626323.RAtIipHOWS5ItinuEdtcoYkQG7gVijDTj8rL0x0_V08CI130_assertion description "[A novel mutation c.118delA in exon 1 of the androgen receptor gene resulting in complete androgen insensitivity syndrome within a large family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626323.RAtIipHOWS5ItinuEdtcoYkQG7gVijDTj8rL0x0_V08CI130_provenance.