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- source_evidence_literature type ECO_0000212 NP1293232.RAyM-iE2Ak2gFpNnugUMmU4RAl5_hAxSgGKCVbNnP0V6s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293232.RAyM-iE2Ak2gFpNnugUMmU4RAl5_hAxSgGKCVbNnP0V6s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293232.RAyM-iE2Ak2gFpNnugUMmU4RAl5_hAxSgGKCVbNnP0V6s130_provenance.
- NP1293232.RAyM-iE2Ak2gFpNnugUMmU4RAl5_hAxSgGKCVbNnP0V6s130_assertion description "[C9orf72 mutations are the most common cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293232.RAyM-iE2Ak2gFpNnugUMmU4RAl5_hAxSgGKCVbNnP0V6s130_provenance.
- NP1293232.RAyM-iE2Ak2gFpNnugUMmU4RAl5_hAxSgGKCVbNnP0V6s130_assertion evidence source_evidence_literature NP1293232.RAyM-iE2Ak2gFpNnugUMmU4RAl5_hAxSgGKCVbNnP0V6s130_provenance.
- NP1293232.RAyM-iE2Ak2gFpNnugUMmU4RAl5_hAxSgGKCVbNnP0V6s130_assertion SIO_000772 26308983 NP1293232.RAyM-iE2Ak2gFpNnugUMmU4RAl5_hAxSgGKCVbNnP0V6s130_provenance.
- NP1293232.RAyM-iE2Ak2gFpNnugUMmU4RAl5_hAxSgGKCVbNnP0V6s130_assertion wasDerivedFrom befree-2016 NP1293232.RAyM-iE2Ak2gFpNnugUMmU4RAl5_hAxSgGKCVbNnP0V6s130_provenance.
- NP1293232.RAyM-iE2Ak2gFpNnugUMmU4RAl5_hAxSgGKCVbNnP0V6s130_assertion wasGeneratedBy ECO_0000203 NP1293232.RAyM-iE2Ak2gFpNnugUMmU4RAl5_hAxSgGKCVbNnP0V6s130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293232.RAyM-iE2Ak2gFpNnugUMmU4RAl5_hAxSgGKCVbNnP0V6s130_provenance.