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- source_evidence_literature type ECO_0000212 NP223765.RAh-5jV2P0f9oRI5wzjS7YqobjB_U-7yBiSVmI8-tndrI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP223765.RAh-5jV2P0f9oRI5wzjS7YqobjB_U-7yBiSVmI8-tndrI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP223765.RAh-5jV2P0f9oRI5wzjS7YqobjB_U-7yBiSVmI8-tndrI130_provenance.
- NP223765.RAh-5jV2P0f9oRI5wzjS7YqobjB_U-7yBiSVmI8-tndrI130_assertion description "[SF1 mutations causing adrenal failure in humans are rare and are more likely to be associated with significant underandrogenization and gonadal dysfunction in 46,XY individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP223765.RAh-5jV2P0f9oRI5wzjS7YqobjB_U-7yBiSVmI8-tndrI130_provenance.
- NP223765.RAh-5jV2P0f9oRI5wzjS7YqobjB_U-7yBiSVmI8-tndrI130_assertion evidence source_evidence_literature NP223765.RAh-5jV2P0f9oRI5wzjS7YqobjB_U-7yBiSVmI8-tndrI130_provenance.
- NP223765.RAh-5jV2P0f9oRI5wzjS7YqobjB_U-7yBiSVmI8-tndrI130_assertion SIO_000772 16684822 NP223765.RAh-5jV2P0f9oRI5wzjS7YqobjB_U-7yBiSVmI8-tndrI130_provenance.
- NP223765.RAh-5jV2P0f9oRI5wzjS7YqobjB_U-7yBiSVmI8-tndrI130_assertion wasDerivedFrom befree-20140225 NP223765.RAh-5jV2P0f9oRI5wzjS7YqobjB_U-7yBiSVmI8-tndrI130_provenance.
- NP223765.RAh-5jV2P0f9oRI5wzjS7YqobjB_U-7yBiSVmI8-tndrI130_assertion wasGeneratedBy ECO_0000203 NP223765.RAh-5jV2P0f9oRI5wzjS7YqobjB_U-7yBiSVmI8-tndrI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP223765.RAh-5jV2P0f9oRI5wzjS7YqobjB_U-7yBiSVmI8-tndrI130_provenance.