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- source_evidence_literature type ECO_0000212 NP139308.RA25vykEGLbnzRRu-ofatW__fwg7JgntLqSowOTahdghE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP139308.RA25vykEGLbnzRRu-ofatW__fwg7JgntLqSowOTahdghE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP139308.RA25vykEGLbnzRRu-ofatW__fwg7JgntLqSowOTahdghE130_provenance.
- NP139308.RA25vykEGLbnzRRu-ofatW__fwg7JgntLqSowOTahdghE130_assertion description "[High frequency of connexin26 (GJB2) mutations associated with nonsyndromic hearing loss in the population of Kerala, India.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP139308.RA25vykEGLbnzRRu-ofatW__fwg7JgntLqSowOTahdghE130_provenance.
- NP139308.RA25vykEGLbnzRRu-ofatW__fwg7JgntLqSowOTahdghE130_assertion evidence source_evidence_literature NP139308.RA25vykEGLbnzRRu-ofatW__fwg7JgntLqSowOTahdghE130_provenance.
- NP139308.RA25vykEGLbnzRRu-ofatW__fwg7JgntLqSowOTahdghE130_assertion SIO_000772 19157576 NP139308.RA25vykEGLbnzRRu-ofatW__fwg7JgntLqSowOTahdghE130_provenance.
- NP139308.RA25vykEGLbnzRRu-ofatW__fwg7JgntLqSowOTahdghE130_assertion wasDerivedFrom gad-20150221 NP139308.RA25vykEGLbnzRRu-ofatW__fwg7JgntLqSowOTahdghE130_provenance.
- NP139308.RA25vykEGLbnzRRu-ofatW__fwg7JgntLqSowOTahdghE130_assertion wasGeneratedBy ECO_0000203 NP139308.RA25vykEGLbnzRRu-ofatW__fwg7JgntLqSowOTahdghE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP139308.RA25vykEGLbnzRRu-ofatW__fwg7JgntLqSowOTahdghE130_provenance.