Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP261311.RA4rLuXrC1T48YVUCrQg_J60rStd5XE0QOYElyg5BKXI8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP261311.RA4rLuXrC1T48YVUCrQg_J60rStd5XE0QOYElyg5BKXI8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP261311.RA4rLuXrC1T48YVUCrQg_J60rStd5XE0QOYElyg5BKXI8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP261311.RA4rLuXrC1T48YVUCrQg_J60rStd5XE0QOYElyg5BKXI8130_provenance.
- NP261311.RA4rLuXrC1T48YVUCrQg_J60rStd5XE0QOYElyg5BKXI8130_assertion description "[This deleted region is close to hSNF5/INI1 (SMARCB1), a gene that encodes a widely expressed component of the SWI/SNF chromatin remodeling complex and that suffers biallelic mutations in malignant rhabdoid tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261311.RA4rLuXrC1T48YVUCrQg_J60rStd5XE0QOYElyg5BKXI8130_provenance.
- NP261311.RA4rLuXrC1T48YVUCrQg_J60rStd5XE0QOYElyg5BKXI8130_assertion evidence source_evidence_literature NP261311.RA4rLuXrC1T48YVUCrQg_J60rStd5XE0QOYElyg5BKXI8130_provenance.
- NP261311.RA4rLuXrC1T48YVUCrQg_J60rStd5XE0QOYElyg5BKXI8130_assertion SIO_000772 10463572 NP261311.RA4rLuXrC1T48YVUCrQg_J60rStd5XE0QOYElyg5BKXI8130_provenance.
- NP261311.RA4rLuXrC1T48YVUCrQg_J60rStd5XE0QOYElyg5BKXI8130_assertion wasDerivedFrom befree-2016 NP261311.RA4rLuXrC1T48YVUCrQg_J60rStd5XE0QOYElyg5BKXI8130_provenance.
- NP261311.RA4rLuXrC1T48YVUCrQg_J60rStd5XE0QOYElyg5BKXI8130_assertion wasGeneratedBy ECO_0000203 NP261311.RA4rLuXrC1T48YVUCrQg_J60rStd5XE0QOYElyg5BKXI8130_provenance.
- befree-2016 importedOn "2016-02-19" NP261311.RA4rLuXrC1T48YVUCrQg_J60rStd5XE0QOYElyg5BKXI8130_provenance.