Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_provenance.
- NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_assertion description "[Hexanucleotide repeat expansions of C9orf72 are the most common genetic cause of amyotrophic lateral sclerosis and frontotemporal degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_provenance.
- NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_assertion evidence source_evidence_literature NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_provenance.
- NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_assertion SIO_000772 24806409 NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_provenance.
- NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_assertion wasDerivedFrom befree-2016 NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_provenance.
- NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_assertion wasGeneratedBy ECO_0000203 NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_provenance.