Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP807106.RAzutJNzXh47MuawvoTHK4_n1jN4aGUhxdJ8MB0IZmLhg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP807106.RAzutJNzXh47MuawvoTHK4_n1jN4aGUhxdJ8MB0IZmLhg130_assertion type Assertion NP807106.RAzutJNzXh47MuawvoTHK4_n1jN4aGUhxdJ8MB0IZmLhg130_head.
- NP807106.RAzutJNzXh47MuawvoTHK4_n1jN4aGUhxdJ8MB0IZmLhg130_assertion description "[MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP807106.RAzutJNzXh47MuawvoTHK4_n1jN4aGUhxdJ8MB0IZmLhg130_provenance.
- NP807106.RAzutJNzXh47MuawvoTHK4_n1jN4aGUhxdJ8MB0IZmLhg130_assertion evidence source_evidence_literature NP807106.RAzutJNzXh47MuawvoTHK4_n1jN4aGUhxdJ8MB0IZmLhg130_provenance.
- NP807106.RAzutJNzXh47MuawvoTHK4_n1jN4aGUhxdJ8MB0IZmLhg130_assertion SIO_000772 17427193 NP807106.RAzutJNzXh47MuawvoTHK4_n1jN4aGUhxdJ8MB0IZmLhg130_provenance.
- NP807106.RAzutJNzXh47MuawvoTHK4_n1jN4aGUhxdJ8MB0IZmLhg130_assertion wasDerivedFrom befree-20140225 NP807106.RAzutJNzXh47MuawvoTHK4_n1jN4aGUhxdJ8MB0IZmLhg130_provenance.
- NP807106.RAzutJNzXh47MuawvoTHK4_n1jN4aGUhxdJ8MB0IZmLhg130_assertion wasGeneratedBy ECO_0000203 NP807106.RAzutJNzXh47MuawvoTHK4_n1jN4aGUhxdJ8MB0IZmLhg130_provenance.