Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP194034.RA6EezTd7YmDeXcxWErCSDNQ4He0LmebV7nsoVdeRikUw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP194034.RA6EezTd7YmDeXcxWErCSDNQ4He0LmebV7nsoVdeRikUw130_assertion type Assertion NP194034.RA6EezTd7YmDeXcxWErCSDNQ4He0LmebV7nsoVdeRikUw130_head.
- NP194034.RA6EezTd7YmDeXcxWErCSDNQ4He0LmebV7nsoVdeRikUw130_assertion wasGeneratedBy ECO_0000203 NP194034.RA6EezTd7YmDeXcxWErCSDNQ4He0LmebV7nsoVdeRikUw130_provenance.
- NP194034.RA6EezTd7YmDeXcxWErCSDNQ4He0LmebV7nsoVdeRikUw130_assertion wasDerivedFrom befree-20140225 NP194034.RA6EezTd7YmDeXcxWErCSDNQ4He0LmebV7nsoVdeRikUw130_provenance.
- NP194034.RA6EezTd7YmDeXcxWErCSDNQ4He0LmebV7nsoVdeRikUw130_assertion SIO_000772 17216245 NP194034.RA6EezTd7YmDeXcxWErCSDNQ4He0LmebV7nsoVdeRikUw130_provenance.
- NP194034.RA6EezTd7YmDeXcxWErCSDNQ4He0LmebV7nsoVdeRikUw130_assertion evidence source_evidence_literature NP194034.RA6EezTd7YmDeXcxWErCSDNQ4He0LmebV7nsoVdeRikUw130_provenance.
- NP194034.RA6EezTd7YmDeXcxWErCSDNQ4He0LmebV7nsoVdeRikUw130_assertion description "[Lack of NPHP2 mutations in a newborn infant with Joubert syndrome-related disorder presenting as end-stage renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP194034.RA6EezTd7YmDeXcxWErCSDNQ4He0LmebV7nsoVdeRikUw130_provenance.