Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP702683.RAwBkDNMNAiZK9tafk1s5yNhZznSnOJbExaqep6MB-LlI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP702683.RAwBkDNMNAiZK9tafk1s5yNhZznSnOJbExaqep6MB-LlI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP702683.RAwBkDNMNAiZK9tafk1s5yNhZznSnOJbExaqep6MB-LlI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP702683.RAwBkDNMNAiZK9tafk1s5yNhZznSnOJbExaqep6MB-LlI130_provenance.
- NP702683.RAwBkDNMNAiZK9tafk1s5yNhZznSnOJbExaqep6MB-LlI130_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." NP702683.RAwBkDNMNAiZK9tafk1s5yNhZznSnOJbExaqep6MB-LlI130_provenance.
- NP702683.RAwBkDNMNAiZK9tafk1s5yNhZznSnOJbExaqep6MB-LlI130_assertion evidence source_evidence_literature NP702683.RAwBkDNMNAiZK9tafk1s5yNhZznSnOJbExaqep6MB-LlI130_provenance.
- NP702683.RAwBkDNMNAiZK9tafk1s5yNhZznSnOJbExaqep6MB-LlI130_assertion SIO_000772 10463572 NP702683.RAwBkDNMNAiZK9tafk1s5yNhZznSnOJbExaqep6MB-LlI130_provenance.
- NP702683.RAwBkDNMNAiZK9tafk1s5yNhZznSnOJbExaqep6MB-LlI130_assertion wasDerivedFrom befree-20150227 NP702683.RAwBkDNMNAiZK9tafk1s5yNhZznSnOJbExaqep6MB-LlI130_provenance.
- NP702683.RAwBkDNMNAiZK9tafk1s5yNhZznSnOJbExaqep6MB-LlI130_assertion wasGeneratedBy ECO_0000203 NP702683.RAwBkDNMNAiZK9tafk1s5yNhZznSnOJbExaqep6MB-LlI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP702683.RAwBkDNMNAiZK9tafk1s5yNhZznSnOJbExaqep6MB-LlI130_provenance.