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- source_evidence_literature type ECO_0000212 NP926127.RAIaeX_YUTiiSd8uYM7iGTXxZDjha7xB-X6IyRfDAvPDI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP926127.RAIaeX_YUTiiSd8uYM7iGTXxZDjha7xB-X6IyRfDAvPDI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP926127.RAIaeX_YUTiiSd8uYM7iGTXxZDjha7xB-X6IyRfDAvPDI130_provenance.
- NP926127.RAIaeX_YUTiiSd8uYM7iGTXxZDjha7xB-X6IyRfDAvPDI130_assertion description "[This same repeat expansion was identified in the majority of our families with a combined FTD/ALS phenotype and TDP-43-based pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP926127.RAIaeX_YUTiiSd8uYM7iGTXxZDjha7xB-X6IyRfDAvPDI130_provenance.
- NP926127.RAIaeX_YUTiiSd8uYM7iGTXxZDjha7xB-X6IyRfDAvPDI130_assertion evidence source_evidence_literature NP926127.RAIaeX_YUTiiSd8uYM7iGTXxZDjha7xB-X6IyRfDAvPDI130_provenance.
- NP926127.RAIaeX_YUTiiSd8uYM7iGTXxZDjha7xB-X6IyRfDAvPDI130_assertion SIO_000772 21944778 NP926127.RAIaeX_YUTiiSd8uYM7iGTXxZDjha7xB-X6IyRfDAvPDI130_provenance.
- NP926127.RAIaeX_YUTiiSd8uYM7iGTXxZDjha7xB-X6IyRfDAvPDI130_assertion wasDerivedFrom befree-2016 NP926127.RAIaeX_YUTiiSd8uYM7iGTXxZDjha7xB-X6IyRfDAvPDI130_provenance.
- NP926127.RAIaeX_YUTiiSd8uYM7iGTXxZDjha7xB-X6IyRfDAvPDI130_assertion wasGeneratedBy ECO_0000203 NP926127.RAIaeX_YUTiiSd8uYM7iGTXxZDjha7xB-X6IyRfDAvPDI130_provenance.
- befree-2016 importedOn "2016-02-19" NP926127.RAIaeX_YUTiiSd8uYM7iGTXxZDjha7xB-X6IyRfDAvPDI130_provenance.