Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP670144.RAwRv3jWeZ2D9FbE0jC8oDXUFR1JfHJloT6PxZRcqb_xw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP670144.RAwRv3jWeZ2D9FbE0jC8oDXUFR1JfHJloT6PxZRcqb_xw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP670144.RAwRv3jWeZ2D9FbE0jC8oDXUFR1JfHJloT6PxZRcqb_xw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP670144.RAwRv3jWeZ2D9FbE0jC8oDXUFR1JfHJloT6PxZRcqb_xw130_provenance.
- NP670144.RAwRv3jWeZ2D9FbE0jC8oDXUFR1JfHJloT6PxZRcqb_xw130_assertion description "[However, electroclinical descriptions in patients with ISSX carrying ARX mutations are scarce.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670144.RAwRv3jWeZ2D9FbE0jC8oDXUFR1JfHJloT6PxZRcqb_xw130_provenance.
- NP670144.RAwRv3jWeZ2D9FbE0jC8oDXUFR1JfHJloT6PxZRcqb_xw130_assertion evidence source_evidence_literature NP670144.RAwRv3jWeZ2D9FbE0jC8oDXUFR1JfHJloT6PxZRcqb_xw130_provenance.
- NP670144.RAwRv3jWeZ2D9FbE0jC8oDXUFR1JfHJloT6PxZRcqb_xw130_assertion SIO_000772 18468866 NP670144.RAwRv3jWeZ2D9FbE0jC8oDXUFR1JfHJloT6PxZRcqb_xw130_provenance.
- NP670144.RAwRv3jWeZ2D9FbE0jC8oDXUFR1JfHJloT6PxZRcqb_xw130_assertion wasDerivedFrom befree-2016 NP670144.RAwRv3jWeZ2D9FbE0jC8oDXUFR1JfHJloT6PxZRcqb_xw130_provenance.
- NP670144.RAwRv3jWeZ2D9FbE0jC8oDXUFR1JfHJloT6PxZRcqb_xw130_assertion wasGeneratedBy ECO_0000203 NP670144.RAwRv3jWeZ2D9FbE0jC8oDXUFR1JfHJloT6PxZRcqb_xw130_provenance.
- befree-2016 importedOn "2016-02-19" NP670144.RAwRv3jWeZ2D9FbE0jC8oDXUFR1JfHJloT6PxZRcqb_xw130_provenance.