Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP399664.RAaczYcDADNn4C-Wk7LAL0USYfI3NhImT3opJ9oP5evZg130_assertion> ?p ?o ?g. }
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- NP399664.RAaczYcDADNn4C-Wk7LAL0USYfI3NhImT3opJ9oP5evZg130_assertion type Assertion NP399664.RAaczYcDADNn4C-Wk7LAL0USYfI3NhImT3opJ9oP5evZg130_head.
- NP399664.RAaczYcDADNn4C-Wk7LAL0USYfI3NhImT3opJ9oP5evZg130_assertion description "[Mutations in FGFR1/FGF8/PROKR2 contributed to 7.8% of our patients with CPHD/SOD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP399664.RAaczYcDADNn4C-Wk7LAL0USYfI3NhImT3opJ9oP5evZg130_provenance.
- NP399664.RAaczYcDADNn4C-Wk7LAL0USYfI3NhImT3opJ9oP5evZg130_assertion evidence source_evidence_literature NP399664.RAaczYcDADNn4C-Wk7LAL0USYfI3NhImT3opJ9oP5evZg130_provenance.
- NP399664.RAaczYcDADNn4C-Wk7LAL0USYfI3NhImT3opJ9oP5evZg130_assertion SIO_000772 22319038 NP399664.RAaczYcDADNn4C-Wk7LAL0USYfI3NhImT3opJ9oP5evZg130_provenance.
- NP399664.RAaczYcDADNn4C-Wk7LAL0USYfI3NhImT3opJ9oP5evZg130_assertion wasDerivedFrom befree-20150227 NP399664.RAaczYcDADNn4C-Wk7LAL0USYfI3NhImT3opJ9oP5evZg130_provenance.
- NP399664.RAaczYcDADNn4C-Wk7LAL0USYfI3NhImT3opJ9oP5evZg130_assertion wasGeneratedBy ECO_0000203 NP399664.RAaczYcDADNn4C-Wk7LAL0USYfI3NhImT3opJ9oP5evZg130_provenance.