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- source_evidence_literature type ECO_0000212 NP399664.RAaczYcDADNn4C-Wk7LAL0USYfI3NhImT3opJ9oP5evZg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP399664.RAaczYcDADNn4C-Wk7LAL0USYfI3NhImT3opJ9oP5evZg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP399664.RAaczYcDADNn4C-Wk7LAL0USYfI3NhImT3opJ9oP5evZg130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP399664.RAaczYcDADNn4C-Wk7LAL0USYfI3NhImT3opJ9oP5evZg130_provenance.