Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP401669.RAH9yT1W_W6rGVdAqK2mOIHrdDNSNHJu1JFtjRdq3pppU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP401669.RAH9yT1W_W6rGVdAqK2mOIHrdDNSNHJu1JFtjRdq3pppU130_assertion type Assertion NP401669.RAH9yT1W_W6rGVdAqK2mOIHrdDNSNHJu1JFtjRdq3pppU130_head.
- NP401669.RAH9yT1W_W6rGVdAqK2mOIHrdDNSNHJu1JFtjRdq3pppU130_assertion wasGeneratedBy ECO_0000203 NP401669.RAH9yT1W_W6rGVdAqK2mOIHrdDNSNHJu1JFtjRdq3pppU130_provenance.
- NP401669.RAH9yT1W_W6rGVdAqK2mOIHrdDNSNHJu1JFtjRdq3pppU130_assertion wasDerivedFrom befree-20150227 NP401669.RAH9yT1W_W6rGVdAqK2mOIHrdDNSNHJu1JFtjRdq3pppU130_provenance.
- NP401669.RAH9yT1W_W6rGVdAqK2mOIHrdDNSNHJu1JFtjRdq3pppU130_assertion SIO_000772 15282208 NP401669.RAH9yT1W_W6rGVdAqK2mOIHrdDNSNHJu1JFtjRdq3pppU130_provenance.
- NP401669.RAH9yT1W_W6rGVdAqK2mOIHrdDNSNHJu1JFtjRdq3pppU130_assertion evidence source_evidence_literature NP401669.RAH9yT1W_W6rGVdAqK2mOIHrdDNSNHJu1JFtjRdq3pppU130_provenance.
- NP401669.RAH9yT1W_W6rGVdAqK2mOIHrdDNSNHJu1JFtjRdq3pppU130_assertion description "[Gain-of-function missense mutations in FGF receptor 2 (FGFR2) are responsible for a variety of craniosynostosis syndromes including Apert syndrome (AS), Pfeiffer syndrome (PS) and Crouzon syndrome (CS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401669.RAH9yT1W_W6rGVdAqK2mOIHrdDNSNHJu1JFtjRdq3pppU130_provenance.