Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1011729.RAWL1AkgcgJU0DicNJDl0aJMw4BHOX3qP0QoNQWVNqlNg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1011729.RAWL1AkgcgJU0DicNJDl0aJMw4BHOX3qP0QoNQWVNqlNg130_assertion type Assertion NP1011729.RAWL1AkgcgJU0DicNJDl0aJMw4BHOX3qP0QoNQWVNqlNg130_head.
- NP1011729.RAWL1AkgcgJU0DicNJDl0aJMw4BHOX3qP0QoNQWVNqlNg130_assertion description "[This study demonstrates evidence of a novel locus SPG38 for Silver syndrome (SS) and suggests that genetic defects in SPG4 might lead to broad clinical features overlapped with those of SS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011729.RAWL1AkgcgJU0DicNJDl0aJMw4BHOX3qP0QoNQWVNqlNg130_provenance.
- NP1011729.RAWL1AkgcgJU0DicNJDl0aJMw4BHOX3qP0QoNQWVNqlNg130_assertion evidence source_evidence_literature NP1011729.RAWL1AkgcgJU0DicNJDl0aJMw4BHOX3qP0QoNQWVNqlNg130_provenance.
- NP1011729.RAWL1AkgcgJU0DicNJDl0aJMw4BHOX3qP0QoNQWVNqlNg130_assertion SIO_000772 18401025 NP1011729.RAWL1AkgcgJU0DicNJDl0aJMw4BHOX3qP0QoNQWVNqlNg130_provenance.
- NP1011729.RAWL1AkgcgJU0DicNJDl0aJMw4BHOX3qP0QoNQWVNqlNg130_assertion wasDerivedFrom befree-20150227 NP1011729.RAWL1AkgcgJU0DicNJDl0aJMw4BHOX3qP0QoNQWVNqlNg130_provenance.
- NP1011729.RAWL1AkgcgJU0DicNJDl0aJMw4BHOX3qP0QoNQWVNqlNg130_assertion wasGeneratedBy ECO_0000203 NP1011729.RAWL1AkgcgJU0DicNJDl0aJMw4BHOX3qP0QoNQWVNqlNg130_provenance.