Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_assertion> ?p ?o ?g. }
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- NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_assertion type Assertion NP1180351.RAHhX0uJrQdZRiwlYwdGcu6NvbvHFr04Lsrn-kV6dLtFs130_head.
- 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.