Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP601938.RA8BkxJiC6s7mPvx2lbXcHj4lW91EDI8eLKR-lGxtnRtE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP601938.RA8BkxJiC6s7mPvx2lbXcHj4lW91EDI8eLKR-lGxtnRtE130_assertion type Assertion NP601938.RA8BkxJiC6s7mPvx2lbXcHj4lW91EDI8eLKR-lGxtnRtE130_head.
- NP601938.RA8BkxJiC6s7mPvx2lbXcHj4lW91EDI8eLKR-lGxtnRtE130_assertion description "[Primary pigmented nodular adrenocortical disease (PPNAD) and pituitary adenoma in a boy with sporadic Carney complex due to a novel, de novo paternal PRKAR1A mutation (R96X).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601938.RA8BkxJiC6s7mPvx2lbXcHj4lW91EDI8eLKR-lGxtnRtE130_provenance.
- NP601938.RA8BkxJiC6s7mPvx2lbXcHj4lW91EDI8eLKR-lGxtnRtE130_assertion evidence source_evidence_literature NP601938.RA8BkxJiC6s7mPvx2lbXcHj4lW91EDI8eLKR-lGxtnRtE130_provenance.
- NP601938.RA8BkxJiC6s7mPvx2lbXcHj4lW91EDI8eLKR-lGxtnRtE130_assertion SIO_000772 17396442 NP601938.RA8BkxJiC6s7mPvx2lbXcHj4lW91EDI8eLKR-lGxtnRtE130_provenance.
- NP601938.RA8BkxJiC6s7mPvx2lbXcHj4lW91EDI8eLKR-lGxtnRtE130_assertion wasDerivedFrom befree-2016 NP601938.RA8BkxJiC6s7mPvx2lbXcHj4lW91EDI8eLKR-lGxtnRtE130_provenance.
- NP601938.RA8BkxJiC6s7mPvx2lbXcHj4lW91EDI8eLKR-lGxtnRtE130_assertion wasGeneratedBy ECO_0000203 NP601938.RA8BkxJiC6s7mPvx2lbXcHj4lW91EDI8eLKR-lGxtnRtE130_provenance.