Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP182301.RAN7_57ummaiWLhBv8NJa8bLmZkjTqv-t6JZSBW9-e6ok130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP182301.RAN7_57ummaiWLhBv8NJa8bLmZkjTqv-t6JZSBW9-e6ok130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP182301.RAN7_57ummaiWLhBv8NJa8bLmZkjTqv-t6JZSBW9-e6ok130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP182301.RAN7_57ummaiWLhBv8NJa8bLmZkjTqv-t6JZSBW9-e6ok130_provenance.
- NP182301.RAN7_57ummaiWLhBv8NJa8bLmZkjTqv-t6JZSBW9-e6ok130_assertion description "[FGFR1 and FGFR2 mutations in Pfeiffer syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182301.RAN7_57ummaiWLhBv8NJa8bLmZkjTqv-t6JZSBW9-e6ok130_provenance.
- NP182301.RAN7_57ummaiWLhBv8NJa8bLmZkjTqv-t6JZSBW9-e6ok130_assertion evidence source_evidence_literature NP182301.RAN7_57ummaiWLhBv8NJa8bLmZkjTqv-t6JZSBW9-e6ok130_provenance.
- NP182301.RAN7_57ummaiWLhBv8NJa8bLmZkjTqv-t6JZSBW9-e6ok130_assertion SIO_000772 23348274 NP182301.RAN7_57ummaiWLhBv8NJa8bLmZkjTqv-t6JZSBW9-e6ok130_provenance.
- NP182301.RAN7_57ummaiWLhBv8NJa8bLmZkjTqv-t6JZSBW9-e6ok130_assertion wasDerivedFrom befree-20140225 NP182301.RAN7_57ummaiWLhBv8NJa8bLmZkjTqv-t6JZSBW9-e6ok130_provenance.
- NP182301.RAN7_57ummaiWLhBv8NJa8bLmZkjTqv-t6JZSBW9-e6ok130_assertion wasGeneratedBy ECO_0000203 NP182301.RAN7_57ummaiWLhBv8NJa8bLmZkjTqv-t6JZSBW9-e6ok130_provenance.
- befree-20140225 importedOn "2014-02-25" NP182301.RAN7_57ummaiWLhBv8NJa8bLmZkjTqv-t6JZSBW9-e6ok130_provenance.