Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP401638.RAFCm5SnooFgrtVp9Zm5B1lvaF2IWEs_70XJHMJzGqmbc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP401638.RAFCm5SnooFgrtVp9Zm5B1lvaF2IWEs_70XJHMJzGqmbc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP401638.RAFCm5SnooFgrtVp9Zm5B1lvaF2IWEs_70XJHMJzGqmbc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP401638.RAFCm5SnooFgrtVp9Zm5B1lvaF2IWEs_70XJHMJzGqmbc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP401638.RAFCm5SnooFgrtVp9Zm5B1lvaF2IWEs_70XJHMJzGqmbc130_provenance.
- NP401638.RAFCm5SnooFgrtVp9Zm5B1lvaF2IWEs_70XJHMJzGqmbc130_assertion wasGeneratedBy ECO_0000203 NP401638.RAFCm5SnooFgrtVp9Zm5B1lvaF2IWEs_70XJHMJzGqmbc130_provenance.
- NP401638.RAFCm5SnooFgrtVp9Zm5B1lvaF2IWEs_70XJHMJzGqmbc130_assertion wasDerivedFrom befree-20150227 NP401638.RAFCm5SnooFgrtVp9Zm5B1lvaF2IWEs_70XJHMJzGqmbc130_provenance.
- NP401638.RAFCm5SnooFgrtVp9Zm5B1lvaF2IWEs_70XJHMJzGqmbc130_assertion SIO_000772 15282208 NP401638.RAFCm5SnooFgrtVp9Zm5B1lvaF2IWEs_70XJHMJzGqmbc130_provenance.
- NP401638.RAFCm5SnooFgrtVp9Zm5B1lvaF2IWEs_70XJHMJzGqmbc130_assertion evidence source_evidence_literature NP401638.RAFCm5SnooFgrtVp9Zm5B1lvaF2IWEs_70XJHMJzGqmbc130_provenance.
- NP401638.RAFCm5SnooFgrtVp9Zm5B1lvaF2IWEs_70XJHMJzGqmbc130_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." NP401638.RAFCm5SnooFgrtVp9Zm5B1lvaF2IWEs_70XJHMJzGqmbc130_provenance.