Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP203258.RAX_hUFqEEISzrEijEpeXIg-vQPPfO2UfFzJLH3ap6FAc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP203258.RAX_hUFqEEISzrEijEpeXIg-vQPPfO2UfFzJLH3ap6FAc130_assertion type Assertion NP203258.RAX_hUFqEEISzrEijEpeXIg-vQPPfO2UfFzJLH3ap6FAc130_head.
- NP203258.RAX_hUFqEEISzrEijEpeXIg-vQPPfO2UfFzJLH3ap6FAc130_assertion wasGeneratedBy ECO_0000203 NP203258.RAX_hUFqEEISzrEijEpeXIg-vQPPfO2UfFzJLH3ap6FAc130_provenance.
- NP203258.RAX_hUFqEEISzrEijEpeXIg-vQPPfO2UfFzJLH3ap6FAc130_assertion wasDerivedFrom befree-20140225 NP203258.RAX_hUFqEEISzrEijEpeXIg-vQPPfO2UfFzJLH3ap6FAc130_provenance.
- NP203258.RAX_hUFqEEISzrEijEpeXIg-vQPPfO2UfFzJLH3ap6FAc130_assertion SIO_000772 10698592 NP203258.RAX_hUFqEEISzrEijEpeXIg-vQPPfO2UfFzJLH3ap6FAc130_provenance.
- NP203258.RAX_hUFqEEISzrEijEpeXIg-vQPPfO2UfFzJLH3ap6FAc130_assertion evidence source_evidence_literature NP203258.RAX_hUFqEEISzrEijEpeXIg-vQPPfO2UfFzJLH3ap6FAc130_provenance.
- NP203258.RAX_hUFqEEISzrEijEpeXIg-vQPPfO2UfFzJLH3ap6FAc130_assertion description "[The identification of the gene(s) causing FGD without mutations in the MC2-R and causing the triple A syndrome may reveal novel aspects in cell signalling and neuroendocrinology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP203258.RAX_hUFqEEISzrEijEpeXIg-vQPPfO2UfFzJLH3ap6FAc130_provenance.