Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP452597.RAM2e7_n0oK4Me8JtY4lG1pNgujNrzTLtTvovElXP56RQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP452597.RAM2e7_n0oK4Me8JtY4lG1pNgujNrzTLtTvovElXP56RQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP452597.RAM2e7_n0oK4Me8JtY4lG1pNgujNrzTLtTvovElXP56RQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP452597.RAM2e7_n0oK4Me8JtY4lG1pNgujNrzTLtTvovElXP56RQ130_provenance.
- NP452597.RAM2e7_n0oK4Me8JtY4lG1pNgujNrzTLtTvovElXP56RQ130_assertion description "[The ZRS contains point mutations that segregate with polydactyly in four unrelated families with PPD and in the Hx mouse mutant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP452597.RAM2e7_n0oK4Me8JtY4lG1pNgujNrzTLtTvovElXP56RQ130_provenance.
- NP452597.RAM2e7_n0oK4Me8JtY4lG1pNgujNrzTLtTvovElXP56RQ130_assertion evidence source_evidence_literature NP452597.RAM2e7_n0oK4Me8JtY4lG1pNgujNrzTLtTvovElXP56RQ130_provenance.
- NP452597.RAM2e7_n0oK4Me8JtY4lG1pNgujNrzTLtTvovElXP56RQ130_assertion SIO_000772 12837695 NP452597.RAM2e7_n0oK4Me8JtY4lG1pNgujNrzTLtTvovElXP56RQ130_provenance.
- NP452597.RAM2e7_n0oK4Me8JtY4lG1pNgujNrzTLtTvovElXP56RQ130_assertion wasDerivedFrom befree-20140225 NP452597.RAM2e7_n0oK4Me8JtY4lG1pNgujNrzTLtTvovElXP56RQ130_provenance.
- NP452597.RAM2e7_n0oK4Me8JtY4lG1pNgujNrzTLtTvovElXP56RQ130_assertion wasGeneratedBy ECO_0000203 NP452597.RAM2e7_n0oK4Me8JtY4lG1pNgujNrzTLtTvovElXP56RQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP452597.RAM2e7_n0oK4Me8JtY4lG1pNgujNrzTLtTvovElXP56RQ130_provenance.