Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP890730.RAuv10UEu05cBfYqWvKQh8RClxbxeorLs5kT9lgBqNsuE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP890730.RAuv10UEu05cBfYqWvKQh8RClxbxeorLs5kT9lgBqNsuE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP890730.RAuv10UEu05cBfYqWvKQh8RClxbxeorLs5kT9lgBqNsuE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP890730.RAuv10UEu05cBfYqWvKQh8RClxbxeorLs5kT9lgBqNsuE130_provenance.
- NP890730.RAuv10UEu05cBfYqWvKQh8RClxbxeorLs5kT9lgBqNsuE130_assertion description "[We recently identified mutations of ARX in nine genotypic males with X-linked lissencephaly with abnormal genitalia (XLAG), and in several female relatives with isolated agenesis of the corpus callosum (ACC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP890730.RAuv10UEu05cBfYqWvKQh8RClxbxeorLs5kT9lgBqNsuE130_provenance.
- NP890730.RAuv10UEu05cBfYqWvKQh8RClxbxeorLs5kT9lgBqNsuE130_assertion evidence source_evidence_literature NP890730.RAuv10UEu05cBfYqWvKQh8RClxbxeorLs5kT9lgBqNsuE130_provenance.
- NP890730.RAuv10UEu05cBfYqWvKQh8RClxbxeorLs5kT9lgBqNsuE130_assertion SIO_000772 14722918 NP890730.RAuv10UEu05cBfYqWvKQh8RClxbxeorLs5kT9lgBqNsuE130_provenance.
- NP890730.RAuv10UEu05cBfYqWvKQh8RClxbxeorLs5kT9lgBqNsuE130_assertion wasDerivedFrom befree-20140225 NP890730.RAuv10UEu05cBfYqWvKQh8RClxbxeorLs5kT9lgBqNsuE130_provenance.
- NP890730.RAuv10UEu05cBfYqWvKQh8RClxbxeorLs5kT9lgBqNsuE130_assertion wasGeneratedBy ECO_0000203 NP890730.RAuv10UEu05cBfYqWvKQh8RClxbxeorLs5kT9lgBqNsuE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP890730.RAuv10UEu05cBfYqWvKQh8RClxbxeorLs5kT9lgBqNsuE130_provenance.