Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_provenance.
- NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_assertion description "[Deletions and inactivating mutations of FOXG1 have been associated with a Rett-like syndrome characterized by hypotonia, irritability, developmental delay, hand stereotypies, and deceleration of head growth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_provenance.
- NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_assertion evidence source_evidence_literature NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_provenance.
- NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_assertion SIO_000772 20736978 NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_provenance.
- NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_assertion wasDerivedFrom befree-20140225 NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_provenance.
- NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_assertion wasGeneratedBy ECO_0000203 NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP654048.RAc2pVkZhaPSCYHq0Gd_Y3i0AWPHfCmY93OMQLZ9TQWeI130_provenance.