Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_assertion type Assertion NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_head.
- NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_assertion wasGeneratedBy ECO_0000203 NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_provenance.
- NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_assertion wasDerivedFrom befree-20140225 NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_provenance.
- NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_assertion SIO_000772 24001744 NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_provenance.
- NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_assertion evidence source_evidence_literature NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_provenance.
- NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_assertion description "[Heterozygous mutations in NPR2 could be an important cause of nonsyndromic familial short stature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP516955.RAPMv5TUTvl5WpLzXFL_LvhKvEFxnbunsSFIGgYrfByvA130_provenance.