Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP8096.RA_NoqyXl2HmFzIWmtqsVL5ivZQ63vNOZnkQiqN4b3LOw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP8096.RA_NoqyXl2HmFzIWmtqsVL5ivZQ63vNOZnkQiqN4b3LOw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8096.RA_NoqyXl2HmFzIWmtqsVL5ivZQ63vNOZnkQiqN4b3LOw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8096.RA_NoqyXl2HmFzIWmtqsVL5ivZQ63vNOZnkQiqN4b3LOw130_provenance.
- NP8096.RA_NoqyXl2HmFzIWmtqsVL5ivZQ63vNOZnkQiqN4b3LOw130_assertion description "[Novel mutations in the DYNC1H1 tail domain refine the genetic and clinical spectrum of dyneinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8096.RA_NoqyXl2HmFzIWmtqsVL5ivZQ63vNOZnkQiqN4b3LOw130_provenance.
- NP8096.RA_NoqyXl2HmFzIWmtqsVL5ivZQ63vNOZnkQiqN4b3LOw130_assertion evidence source_evidence_curated NP8096.RA_NoqyXl2HmFzIWmtqsVL5ivZQ63vNOZnkQiqN4b3LOw130_provenance.
- NP8096.RA_NoqyXl2HmFzIWmtqsVL5ivZQ63vNOZnkQiqN4b3LOw130_assertion SIO_000772 25512093 NP8096.RA_NoqyXl2HmFzIWmtqsVL5ivZQ63vNOZnkQiqN4b3LOw130_provenance.
- NP8096.RA_NoqyXl2HmFzIWmtqsVL5ivZQ63vNOZnkQiqN4b3LOw130_assertion wasDerivedFrom uniprot-2016 NP8096.RA_NoqyXl2HmFzIWmtqsVL5ivZQ63vNOZnkQiqN4b3LOw130_provenance.
- NP8096.RA_NoqyXl2HmFzIWmtqsVL5ivZQ63vNOZnkQiqN4b3LOw130_assertion wasGeneratedBy ECO_0000218 NP8096.RA_NoqyXl2HmFzIWmtqsVL5ivZQ63vNOZnkQiqN4b3LOw130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP8096.RA_NoqyXl2HmFzIWmtqsVL5ivZQ63vNOZnkQiqN4b3LOw130_provenance.