Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP803441.RAWs44693FKceQn3yjHWfQlQJBswZ8_b6d8qWZic1R61s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP803441.RAWs44693FKceQn3yjHWfQlQJBswZ8_b6d8qWZic1R61s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP803441.RAWs44693FKceQn3yjHWfQlQJBswZ8_b6d8qWZic1R61s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP803441.RAWs44693FKceQn3yjHWfQlQJBswZ8_b6d8qWZic1R61s130_provenance.
- NP803441.RAWs44693FKceQn3yjHWfQlQJBswZ8_b6d8qWZic1R61s130_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." NP803441.RAWs44693FKceQn3yjHWfQlQJBswZ8_b6d8qWZic1R61s130_provenance.
- NP803441.RAWs44693FKceQn3yjHWfQlQJBswZ8_b6d8qWZic1R61s130_assertion evidence source_evidence_literature NP803441.RAWs44693FKceQn3yjHWfQlQJBswZ8_b6d8qWZic1R61s130_provenance.
- NP803441.RAWs44693FKceQn3yjHWfQlQJBswZ8_b6d8qWZic1R61s130_assertion SIO_000772 12837695 NP803441.RAWs44693FKceQn3yjHWfQlQJBswZ8_b6d8qWZic1R61s130_provenance.
- NP803441.RAWs44693FKceQn3yjHWfQlQJBswZ8_b6d8qWZic1R61s130_assertion wasDerivedFrom befree-20140225 NP803441.RAWs44693FKceQn3yjHWfQlQJBswZ8_b6d8qWZic1R61s130_provenance.
- NP803441.RAWs44693FKceQn3yjHWfQlQJBswZ8_b6d8qWZic1R61s130_assertion wasGeneratedBy ECO_0000203 NP803441.RAWs44693FKceQn3yjHWfQlQJBswZ8_b6d8qWZic1R61s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP803441.RAWs44693FKceQn3yjHWfQlQJBswZ8_b6d8qWZic1R61s130_provenance.