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- source_evidence_literature type ECO_0000212 NP559765.RAbfyO4YVY-nFbMVkwfEkI7qy8QwvaiXUliFJuEyAmo2k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP559765.RAbfyO4YVY-nFbMVkwfEkI7qy8QwvaiXUliFJuEyAmo2k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP559765.RAbfyO4YVY-nFbMVkwfEkI7qy8QwvaiXUliFJuEyAmo2k130_provenance.
- NP559765.RAbfyO4YVY-nFbMVkwfEkI7qy8QwvaiXUliFJuEyAmo2k130_assertion description "[Structural chromosome disruption of the NR3C2 gene causing pseudohypoaldosteronism type 1 presenting in infancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP559765.RAbfyO4YVY-nFbMVkwfEkI7qy8QwvaiXUliFJuEyAmo2k130_provenance.
- NP559765.RAbfyO4YVY-nFbMVkwfEkI7qy8QwvaiXUliFJuEyAmo2k130_assertion evidence source_evidence_literature NP559765.RAbfyO4YVY-nFbMVkwfEkI7qy8QwvaiXUliFJuEyAmo2k130_provenance.
- NP559765.RAbfyO4YVY-nFbMVkwfEkI7qy8QwvaiXUliFJuEyAmo2k130_assertion SIO_000772 21932599 NP559765.RAbfyO4YVY-nFbMVkwfEkI7qy8QwvaiXUliFJuEyAmo2k130_provenance.
- NP559765.RAbfyO4YVY-nFbMVkwfEkI7qy8QwvaiXUliFJuEyAmo2k130_assertion wasDerivedFrom befree-20150227 NP559765.RAbfyO4YVY-nFbMVkwfEkI7qy8QwvaiXUliFJuEyAmo2k130_provenance.
- NP559765.RAbfyO4YVY-nFbMVkwfEkI7qy8QwvaiXUliFJuEyAmo2k130_assertion wasGeneratedBy ECO_0000203 NP559765.RAbfyO4YVY-nFbMVkwfEkI7qy8QwvaiXUliFJuEyAmo2k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP559765.RAbfyO4YVY-nFbMVkwfEkI7qy8QwvaiXUliFJuEyAmo2k130_provenance.