Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP979847.RApLzRySKyHHJmK4RYpKEyWD4LluXfM72xF0J1XRE9mhY130_assertion> ?p ?o ?g. }
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- NP979847.RApLzRySKyHHJmK4RYpKEyWD4LluXfM72xF0J1XRE9mhY130_assertion type Assertion NP979847.RApLzRySKyHHJmK4RYpKEyWD4LluXfM72xF0J1XRE9mhY130_head.
- NP979847.RApLzRySKyHHJmK4RYpKEyWD4LluXfM72xF0J1XRE9mhY130_assertion description "[We developed gene panel based technologies to assess 16 genes known to harbour mutations causal of dementia and combined these with PCR based assessments of the C9orf72 hexanucleotide repeat expansion and the octapeptide repeat region of PRNP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP979847.RApLzRySKyHHJmK4RYpKEyWD4LluXfM72xF0J1XRE9mhY130_provenance.
- NP979847.RApLzRySKyHHJmK4RYpKEyWD4LluXfM72xF0J1XRE9mhY130_assertion evidence source_evidence_literature NP979847.RApLzRySKyHHJmK4RYpKEyWD4LluXfM72xF0J1XRE9mhY130_provenance.
- NP979847.RApLzRySKyHHJmK4RYpKEyWD4LluXfM72xF0J1XRE9mhY130_assertion SIO_000772 23998997 NP979847.RApLzRySKyHHJmK4RYpKEyWD4LluXfM72xF0J1XRE9mhY130_provenance.
- NP979847.RApLzRySKyHHJmK4RYpKEyWD4LluXfM72xF0J1XRE9mhY130_assertion wasDerivedFrom befree-20150227 NP979847.RApLzRySKyHHJmK4RYpKEyWD4LluXfM72xF0J1XRE9mhY130_provenance.
- NP979847.RApLzRySKyHHJmK4RYpKEyWD4LluXfM72xF0J1XRE9mhY130_assertion wasGeneratedBy ECO_0000203 NP979847.RApLzRySKyHHJmK4RYpKEyWD4LluXfM72xF0J1XRE9mhY130_provenance.