Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP500022.RAco3ST3sK_V8OujqF1MrfeUsviz9gmilTpHlNsR1x0hw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP500022.RAco3ST3sK_V8OujqF1MrfeUsviz9gmilTpHlNsR1x0hw130_assertion type Assertion NP500022.RAco3ST3sK_V8OujqF1MrfeUsviz9gmilTpHlNsR1x0hw130_head.
- NP500022.RAco3ST3sK_V8OujqF1MrfeUsviz9gmilTpHlNsR1x0hw130_assertion description "[PROP1 mutations can be associated with a highly variable phenotype, and both pituitary hypoplasia and pituitary hyperplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500022.RAco3ST3sK_V8OujqF1MrfeUsviz9gmilTpHlNsR1x0hw130_provenance.
- NP500022.RAco3ST3sK_V8OujqF1MrfeUsviz9gmilTpHlNsR1x0hw130_assertion evidence source_evidence_literature NP500022.RAco3ST3sK_V8OujqF1MrfeUsviz9gmilTpHlNsR1x0hw130_provenance.
- NP500022.RAco3ST3sK_V8OujqF1MrfeUsviz9gmilTpHlNsR1x0hw130_assertion SIO_000772 15963055 NP500022.RAco3ST3sK_V8OujqF1MrfeUsviz9gmilTpHlNsR1x0hw130_provenance.
- NP500022.RAco3ST3sK_V8OujqF1MrfeUsviz9gmilTpHlNsR1x0hw130_assertion wasDerivedFrom befree-2016 NP500022.RAco3ST3sK_V8OujqF1MrfeUsviz9gmilTpHlNsR1x0hw130_provenance.
- NP500022.RAco3ST3sK_V8OujqF1MrfeUsviz9gmilTpHlNsR1x0hw130_assertion wasGeneratedBy ECO_0000203 NP500022.RAco3ST3sK_V8OujqF1MrfeUsviz9gmilTpHlNsR1x0hw130_provenance.