Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_assertion type Assertion NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_head.
- NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_assertion description "[Mutational analysis of the RSPO1 gene in a 46, XX woman with true hermaphroditism, palmoplantar keratoderma, congenital bilateral corneal opacities, onychodystrophy, and hearing impairment, is reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_provenance.
- NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_assertion evidence source_evidence_literature NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_provenance.
- NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_assertion SIO_000772 18085567 NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_provenance.
- NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_assertion wasDerivedFrom lhgdn-20090331 NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_provenance.
- NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_assertion wasGeneratedBy ECO_0000203 NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_provenance.