Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP647655.RAVTAV1QvEYD1w8AgHZNOqem9vccrw9I5zUv9Ft9aLQWk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP647655.RAVTAV1QvEYD1w8AgHZNOqem9vccrw9I5zUv9Ft9aLQWk130_assertion type Assertion NP647655.RAVTAV1QvEYD1w8AgHZNOqem9vccrw9I5zUv9Ft9aLQWk130_head.
- NP647655.RAVTAV1QvEYD1w8AgHZNOqem9vccrw9I5zUv9Ft9aLQWk130_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." NP647655.RAVTAV1QvEYD1w8AgHZNOqem9vccrw9I5zUv9Ft9aLQWk130_provenance.
- NP647655.RAVTAV1QvEYD1w8AgHZNOqem9vccrw9I5zUv9Ft9aLQWk130_assertion evidence source_evidence_literature NP647655.RAVTAV1QvEYD1w8AgHZNOqem9vccrw9I5zUv9Ft9aLQWk130_provenance.
- NP647655.RAVTAV1QvEYD1w8AgHZNOqem9vccrw9I5zUv9Ft9aLQWk130_assertion SIO_000772 23998997 NP647655.RAVTAV1QvEYD1w8AgHZNOqem9vccrw9I5zUv9Ft9aLQWk130_provenance.
- NP647655.RAVTAV1QvEYD1w8AgHZNOqem9vccrw9I5zUv9Ft9aLQWk130_assertion wasDerivedFrom befree-20150227 NP647655.RAVTAV1QvEYD1w8AgHZNOqem9vccrw9I5zUv9Ft9aLQWk130_provenance.
- NP647655.RAVTAV1QvEYD1w8AgHZNOqem9vccrw9I5zUv9Ft9aLQWk130_assertion wasGeneratedBy ECO_0000203 NP647655.RAVTAV1QvEYD1w8AgHZNOqem9vccrw9I5zUv9Ft9aLQWk130_provenance.