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- source_evidence_literature type ECO_0000212 NP1404313.RA5nyXxOHORMqVf8gykXuaAXPjQzwrX4K-YIG4TyZs2fY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1404313.RA5nyXxOHORMqVf8gykXuaAXPjQzwrX4K-YIG4TyZs2fY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1404313.RA5nyXxOHORMqVf8gykXuaAXPjQzwrX4K-YIG4TyZs2fY130_provenance.
- NP1404313.RA5nyXxOHORMqVf8gykXuaAXPjQzwrX4K-YIG4TyZs2fY130_assertion description "[We have, therefore, excluded HRY as the gene for dominant optic atrophy by sequence analysis, mapped it genetically, and identified a polymorphism in our population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1404313.RA5nyXxOHORMqVf8gykXuaAXPjQzwrX4K-YIG4TyZs2fY130_provenance.
- NP1404313.RA5nyXxOHORMqVf8gykXuaAXPjQzwrX4K-YIG4TyZs2fY130_assertion evidence source_evidence_literature NP1404313.RA5nyXxOHORMqVf8gykXuaAXPjQzwrX4K-YIG4TyZs2fY130_provenance.
- NP1404313.RA5nyXxOHORMqVf8gykXuaAXPjQzwrX4K-YIG4TyZs2fY130_assertion SIO_000772 9745030 NP1404313.RA5nyXxOHORMqVf8gykXuaAXPjQzwrX4K-YIG4TyZs2fY130_provenance.
- NP1404313.RA5nyXxOHORMqVf8gykXuaAXPjQzwrX4K-YIG4TyZs2fY130_assertion wasDerivedFrom befree-2016 NP1404313.RA5nyXxOHORMqVf8gykXuaAXPjQzwrX4K-YIG4TyZs2fY130_provenance.
- NP1404313.RA5nyXxOHORMqVf8gykXuaAXPjQzwrX4K-YIG4TyZs2fY130_assertion wasGeneratedBy ECO_0000203 NP1404313.RA5nyXxOHORMqVf8gykXuaAXPjQzwrX4K-YIG4TyZs2fY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1404313.RA5nyXxOHORMqVf8gykXuaAXPjQzwrX4K-YIG4TyZs2fY130_provenance.