Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP324910.RAa8Bq2Mp16KrvS7l-oM7xj5xCJWJxbMMZ2AQPJif2boM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP324910.RAa8Bq2Mp16KrvS7l-oM7xj5xCJWJxbMMZ2AQPJif2boM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP324910.RAa8Bq2Mp16KrvS7l-oM7xj5xCJWJxbMMZ2AQPJif2boM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP324910.RAa8Bq2Mp16KrvS7l-oM7xj5xCJWJxbMMZ2AQPJif2boM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP324910.RAa8Bq2Mp16KrvS7l-oM7xj5xCJWJxbMMZ2AQPJif2boM130_provenance.
- NP324910.RAa8Bq2Mp16KrvS7l-oM7xj5xCJWJxbMMZ2AQPJif2boM130_assertion wasGeneratedBy ECO_0000203 NP324910.RAa8Bq2Mp16KrvS7l-oM7xj5xCJWJxbMMZ2AQPJif2boM130_provenance.
- NP324910.RAa8Bq2Mp16KrvS7l-oM7xj5xCJWJxbMMZ2AQPJif2boM130_assertion wasDerivedFrom befree-20150227 NP324910.RAa8Bq2Mp16KrvS7l-oM7xj5xCJWJxbMMZ2AQPJif2boM130_provenance.
- NP324910.RAa8Bq2Mp16KrvS7l-oM7xj5xCJWJxbMMZ2AQPJif2boM130_assertion SIO_000772 9633819 NP324910.RAa8Bq2Mp16KrvS7l-oM7xj5xCJWJxbMMZ2AQPJif2boM130_provenance.
- NP324910.RAa8Bq2Mp16KrvS7l-oM7xj5xCJWJxbMMZ2AQPJif2boM130_assertion evidence source_evidence_literature NP324910.RAa8Bq2Mp16KrvS7l-oM7xj5xCJWJxbMMZ2AQPJif2boM130_provenance.
- NP324910.RAa8Bq2Mp16KrvS7l-oM7xj5xCJWJxbMMZ2AQPJif2boM130_assertion description "[The associated genetic defects characterized revealed compound heterozygosity for a splice defect leading to skipping of exon 8, due to a G-->A transition at position -1 of the exon 8 splice donor site, and a point mutation leading to a Hisl08Pro change (CAT-->CCT) in two patients (siblings) with mild CESD phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324910.RAa8Bq2Mp16KrvS7l-oM7xj5xCJWJxbMMZ2AQPJif2boM130_provenance.