Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP322792.RAmfKzPG1BaYcBsK5XySwc1jQHnlc_H1bRfQxgRT9YFMs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP322792.RAmfKzPG1BaYcBsK5XySwc1jQHnlc_H1bRfQxgRT9YFMs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP322792.RAmfKzPG1BaYcBsK5XySwc1jQHnlc_H1bRfQxgRT9YFMs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP322792.RAmfKzPG1BaYcBsK5XySwc1jQHnlc_H1bRfQxgRT9YFMs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP322792.RAmfKzPG1BaYcBsK5XySwc1jQHnlc_H1bRfQxgRT9YFMs130_provenance.
- NP322792.RAmfKzPG1BaYcBsK5XySwc1jQHnlc_H1bRfQxgRT9YFMs130_assertion wasGeneratedBy ECO_0000203 NP322792.RAmfKzPG1BaYcBsK5XySwc1jQHnlc_H1bRfQxgRT9YFMs130_provenance.
- NP322792.RAmfKzPG1BaYcBsK5XySwc1jQHnlc_H1bRfQxgRT9YFMs130_assertion wasDerivedFrom befree-20150227 NP322792.RAmfKzPG1BaYcBsK5XySwc1jQHnlc_H1bRfQxgRT9YFMs130_provenance.
- NP322792.RAmfKzPG1BaYcBsK5XySwc1jQHnlc_H1bRfQxgRT9YFMs130_assertion SIO_000772 8530067 NP322792.RAmfKzPG1BaYcBsK5XySwc1jQHnlc_H1bRfQxgRT9YFMs130_provenance.
- NP322792.RAmfKzPG1BaYcBsK5XySwc1jQHnlc_H1bRfQxgRT9YFMs130_assertion evidence source_evidence_literature NP322792.RAmfKzPG1BaYcBsK5XySwc1jQHnlc_H1bRfQxgRT9YFMs130_provenance.
- NP322792.RAmfKzPG1BaYcBsK5XySwc1jQHnlc_H1bRfQxgRT9YFMs130_assertion description "[A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsyndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322792.RAmfKzPG1BaYcBsK5XySwc1jQHnlc_H1bRfQxgRT9YFMs130_provenance.