Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP400898.RAPymuFZ06sbOyt8Km78ZNTcot6Wefx99aBhDGFaiReOA130_assertion> ?p ?o ?g. }
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- NP400898.RAPymuFZ06sbOyt8Km78ZNTcot6Wefx99aBhDGFaiReOA130_assertion type Assertion NP400898.RAPymuFZ06sbOyt8Km78ZNTcot6Wefx99aBhDGFaiReOA130_head.
- NP400898.RAPymuFZ06sbOyt8Km78ZNTcot6Wefx99aBhDGFaiReOA130_assertion wasGeneratedBy ECO_0000203 NP400898.RAPymuFZ06sbOyt8Km78ZNTcot6Wefx99aBhDGFaiReOA130_provenance.
- NP400898.RAPymuFZ06sbOyt8Km78ZNTcot6Wefx99aBhDGFaiReOA130_assertion wasDerivedFrom befree-20150227 NP400898.RAPymuFZ06sbOyt8Km78ZNTcot6Wefx99aBhDGFaiReOA130_provenance.
- NP400898.RAPymuFZ06sbOyt8Km78ZNTcot6Wefx99aBhDGFaiReOA130_assertion SIO_000772 19243295 NP400898.RAPymuFZ06sbOyt8Km78ZNTcot6Wefx99aBhDGFaiReOA130_provenance.
- NP400898.RAPymuFZ06sbOyt8Km78ZNTcot6Wefx99aBhDGFaiReOA130_assertion evidence source_evidence_literature NP400898.RAPymuFZ06sbOyt8Km78ZNTcot6Wefx99aBhDGFaiReOA130_provenance.
- NP400898.RAPymuFZ06sbOyt8Km78ZNTcot6Wefx99aBhDGFaiReOA130_assertion description "[The majority of the mutations identified are identical to germline mutations in FGFR2 and FGFR3 that cause craniosynostosis and hypochondroplasia syndromes and result in both ligand-independent and ligand-dependent receptor activation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400898.RAPymuFZ06sbOyt8Km78ZNTcot6Wefx99aBhDGFaiReOA130_provenance.