Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP155636.RANW9XNl2C5LABgE6y1h5P16jQ2EuFzeOsOEFTjMs9uA0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP155636.RANW9XNl2C5LABgE6y1h5P16jQ2EuFzeOsOEFTjMs9uA0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP155636.RANW9XNl2C5LABgE6y1h5P16jQ2EuFzeOsOEFTjMs9uA0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP155636.RANW9XNl2C5LABgE6y1h5P16jQ2EuFzeOsOEFTjMs9uA0130_provenance.
- NP155636.RANW9XNl2C5LABgE6y1h5P16jQ2EuFzeOsOEFTjMs9uA0130_assertion description "[Single nucleotide polymorphisms and haplotypes analysis of DFNB1 locus in Chinese sporadic hearing impairment population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP155636.RANW9XNl2C5LABgE6y1h5P16jQ2EuFzeOsOEFTjMs9uA0130_provenance.
- NP155636.RANW9XNl2C5LABgE6y1h5P16jQ2EuFzeOsOEFTjMs9uA0130_assertion evidence source_evidence_literature NP155636.RANW9XNl2C5LABgE6y1h5P16jQ2EuFzeOsOEFTjMs9uA0130_provenance.
- NP155636.RANW9XNl2C5LABgE6y1h5P16jQ2EuFzeOsOEFTjMs9uA0130_assertion SIO_000772 19719946 NP155636.RANW9XNl2C5LABgE6y1h5P16jQ2EuFzeOsOEFTjMs9uA0130_provenance.
- NP155636.RANW9XNl2C5LABgE6y1h5P16jQ2EuFzeOsOEFTjMs9uA0130_assertion wasDerivedFrom gad-20150221 NP155636.RANW9XNl2C5LABgE6y1h5P16jQ2EuFzeOsOEFTjMs9uA0130_provenance.
- NP155636.RANW9XNl2C5LABgE6y1h5P16jQ2EuFzeOsOEFTjMs9uA0130_assertion wasGeneratedBy ECO_0000203 NP155636.RANW9XNl2C5LABgE6y1h5P16jQ2EuFzeOsOEFTjMs9uA0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP155636.RANW9XNl2C5LABgE6y1h5P16jQ2EuFzeOsOEFTjMs9uA0130_provenance.