Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP37472.RABYUNSkqPEJHPhQJJiRmhzsbTIaelJUGelz9rRwrTZMM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP37472.RABYUNSkqPEJHPhQJJiRmhzsbTIaelJUGelz9rRwrTZMM130_assertion type Assertion NP37472.RABYUNSkqPEJHPhQJJiRmhzsbTIaelJUGelz9rRwrTZMM130_head.
- NP37472.RABYUNSkqPEJHPhQJJiRmhzsbTIaelJUGelz9rRwrTZMM130_assertion wasGeneratedBy ECO_0000218 NP37472.RABYUNSkqPEJHPhQJJiRmhzsbTIaelJUGelz9rRwrTZMM130_provenance.
- NP37472.RABYUNSkqPEJHPhQJJiRmhzsbTIaelJUGelz9rRwrTZMM130_assertion wasDerivedFrom ctd_human-2016 NP37472.RABYUNSkqPEJHPhQJJiRmhzsbTIaelJUGelz9rRwrTZMM130_provenance.
- NP37472.RABYUNSkqPEJHPhQJJiRmhzsbTIaelJUGelz9rRwrTZMM130_assertion SIO_000772 9152842 NP37472.RABYUNSkqPEJHPhQJJiRmhzsbTIaelJUGelz9rRwrTZMM130_provenance.
- NP37472.RABYUNSkqPEJHPhQJJiRmhzsbTIaelJUGelz9rRwrTZMM130_assertion evidence source_evidence_curated NP37472.RABYUNSkqPEJHPhQJJiRmhzsbTIaelJUGelz9rRwrTZMM130_provenance.
- NP37472.RABYUNSkqPEJHPhQJJiRmhzsbTIaelJUGelz9rRwrTZMM130_assertion description "[A novel mutation (a886g) in exon 5 of FGFR2 in members of a family with Crouzon phenotype and plagiocephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP37472.RABYUNSkqPEJHPhQJJiRmhzsbTIaelJUGelz9rRwrTZMM130_provenance.