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- source_evidence_literature type ECO_0000212 NP978193.RAmi1WyWYuFjf-PHz0j1fagen2KTHb3vHq7h0sHBwahrE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978193.RAmi1WyWYuFjf-PHz0j1fagen2KTHb3vHq7h0sHBwahrE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978193.RAmi1WyWYuFjf-PHz0j1fagen2KTHb3vHq7h0sHBwahrE130_provenance.
- NP978193.RAmi1WyWYuFjf-PHz0j1fagen2KTHb3vHq7h0sHBwahrE130_assertion description "[The authors assessed ARX as a candidate gene for XLAG in a genetic analysis of neuronal migration disorders and found two different point mutations in two XLAG pedigrees affecting the homeodomain of the protein, confirming that ARX is a causative gene for XLAG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978193.RAmi1WyWYuFjf-PHz0j1fagen2KTHb3vHq7h0sHBwahrE130_provenance.
- NP978193.RAmi1WyWYuFjf-PHz0j1fagen2KTHb3vHq7h0sHBwahrE130_assertion evidence source_evidence_literature NP978193.RAmi1WyWYuFjf-PHz0j1fagen2KTHb3vHq7h0sHBwahrE130_provenance.
- NP978193.RAmi1WyWYuFjf-PHz0j1fagen2KTHb3vHq7h0sHBwahrE130_assertion SIO_000772 12874405 NP978193.RAmi1WyWYuFjf-PHz0j1fagen2KTHb3vHq7h0sHBwahrE130_provenance.
- NP978193.RAmi1WyWYuFjf-PHz0j1fagen2KTHb3vHq7h0sHBwahrE130_assertion wasDerivedFrom befree-20150227 NP978193.RAmi1WyWYuFjf-PHz0j1fagen2KTHb3vHq7h0sHBwahrE130_provenance.
- NP978193.RAmi1WyWYuFjf-PHz0j1fagen2KTHb3vHq7h0sHBwahrE130_assertion wasGeneratedBy ECO_0000203 NP978193.RAmi1WyWYuFjf-PHz0j1fagen2KTHb3vHq7h0sHBwahrE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978193.RAmi1WyWYuFjf-PHz0j1fagen2KTHb3vHq7h0sHBwahrE130_provenance.