Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP807106.RAzutJNzXh47MuawvoTHK4_n1jN4aGUhxdJ8MB0IZmLhg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP807106.RAzutJNzXh47MuawvoTHK4_n1jN4aGUhxdJ8MB0IZmLhg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP807106.RAzutJNzXh47MuawvoTHK4_n1jN4aGUhxdJ8MB0IZmLhg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP807106.RAzutJNzXh47MuawvoTHK4_n1jN4aGUhxdJ8MB0IZmLhg130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP807106.RAzutJNzXh47MuawvoTHK4_n1jN4aGUhxdJ8MB0IZmLhg130_provenance.