Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP568616.RA1y-MvkOKrMdTOCdRfb49GstM-_3WXSYXDg-pDobN_cs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP568616.RA1y-MvkOKrMdTOCdRfb49GstM-_3WXSYXDg-pDobN_cs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568616.RA1y-MvkOKrMdTOCdRfb49GstM-_3WXSYXDg-pDobN_cs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568616.RA1y-MvkOKrMdTOCdRfb49GstM-_3WXSYXDg-pDobN_cs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP568616.RA1y-MvkOKrMdTOCdRfb49GstM-_3WXSYXDg-pDobN_cs130_provenance.
- NP568616.RA1y-MvkOKrMdTOCdRfb49GstM-_3WXSYXDg-pDobN_cs130_assertion wasGeneratedBy ECO_0000203 NP568616.RA1y-MvkOKrMdTOCdRfb49GstM-_3WXSYXDg-pDobN_cs130_provenance.
- NP568616.RA1y-MvkOKrMdTOCdRfb49GstM-_3WXSYXDg-pDobN_cs130_assertion wasDerivedFrom befree-20150227 NP568616.RA1y-MvkOKrMdTOCdRfb49GstM-_3WXSYXDg-pDobN_cs130_provenance.
- NP568616.RA1y-MvkOKrMdTOCdRfb49GstM-_3WXSYXDg-pDobN_cs130_assertion SIO_000772 16283678 NP568616.RA1y-MvkOKrMdTOCdRfb49GstM-_3WXSYXDg-pDobN_cs130_provenance.
- NP568616.RA1y-MvkOKrMdTOCdRfb49GstM-_3WXSYXDg-pDobN_cs130_assertion evidence source_evidence_literature NP568616.RA1y-MvkOKrMdTOCdRfb49GstM-_3WXSYXDg-pDobN_cs130_provenance.
- NP568616.RA1y-MvkOKrMdTOCdRfb49GstM-_3WXSYXDg-pDobN_cs130_assertion description "[Most recently, about a dozen other cases of inherited bi-allelic deficiency of mismatch repair (MMR) genes associated with early onset CNS tumors, hematologic malignancy, gastrointestinal neoplasia, café-au-lait spots, and other NF1 features have been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568616.RA1y-MvkOKrMdTOCdRfb49GstM-_3WXSYXDg-pDobN_cs130_provenance.