Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP354964.RAeXFZ8inC927O9MfBHTe5rTY1sEjRv6NIQgKvqfp55YQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP354964.RAeXFZ8inC927O9MfBHTe5rTY1sEjRv6NIQgKvqfp55YQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP354964.RAeXFZ8inC927O9MfBHTe5rTY1sEjRv6NIQgKvqfp55YQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP354964.RAeXFZ8inC927O9MfBHTe5rTY1sEjRv6NIQgKvqfp55YQ130_provenance.
- NP354964.RAeXFZ8inC927O9MfBHTe5rTY1sEjRv6NIQgKvqfp55YQ130_assertion description "[The conclusion that DLX5 is a direct target of MeCP2 has implications for research on the molecular bases of Rett syndrome, autism, and genomic imprinting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354964.RAeXFZ8inC927O9MfBHTe5rTY1sEjRv6NIQgKvqfp55YQ130_provenance.
- NP354964.RAeXFZ8inC927O9MfBHTe5rTY1sEjRv6NIQgKvqfp55YQ130_assertion evidence source_evidence_literature NP354964.RAeXFZ8inC927O9MfBHTe5rTY1sEjRv6NIQgKvqfp55YQ130_provenance.
- NP354964.RAeXFZ8inC927O9MfBHTe5rTY1sEjRv6NIQgKvqfp55YQ130_assertion SIO_000772 17701895 NP354964.RAeXFZ8inC927O9MfBHTe5rTY1sEjRv6NIQgKvqfp55YQ130_provenance.
- NP354964.RAeXFZ8inC927O9MfBHTe5rTY1sEjRv6NIQgKvqfp55YQ130_assertion wasDerivedFrom befree-20150227 NP354964.RAeXFZ8inC927O9MfBHTe5rTY1sEjRv6NIQgKvqfp55YQ130_provenance.
- NP354964.RAeXFZ8inC927O9MfBHTe5rTY1sEjRv6NIQgKvqfp55YQ130_assertion wasGeneratedBy ECO_0000203 NP354964.RAeXFZ8inC927O9MfBHTe5rTY1sEjRv6NIQgKvqfp55YQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP354964.RAeXFZ8inC927O9MfBHTe5rTY1sEjRv6NIQgKvqfp55YQ130_provenance.