Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP754787.RAf7HXKVfIHZpJCVUe5HKmjQXgXbrAW4wro_FoAU_pWDE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP754787.RAf7HXKVfIHZpJCVUe5HKmjQXgXbrAW4wro_FoAU_pWDE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP754787.RAf7HXKVfIHZpJCVUe5HKmjQXgXbrAW4wro_FoAU_pWDE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP754787.RAf7HXKVfIHZpJCVUe5HKmjQXgXbrAW4wro_FoAU_pWDE130_provenance.
- befree-2016 importedOn "2016-02-19" NP754787.RAf7HXKVfIHZpJCVUe5HKmjQXgXbrAW4wro_FoAU_pWDE130_provenance.
- NP754787.RAf7HXKVfIHZpJCVUe5HKmjQXgXbrAW4wro_FoAU_pWDE130_assertion wasGeneratedBy ECO_0000203 NP754787.RAf7HXKVfIHZpJCVUe5HKmjQXgXbrAW4wro_FoAU_pWDE130_provenance.
- NP754787.RAf7HXKVfIHZpJCVUe5HKmjQXgXbrAW4wro_FoAU_pWDE130_assertion wasDerivedFrom befree-2016 NP754787.RAf7HXKVfIHZpJCVUe5HKmjQXgXbrAW4wro_FoAU_pWDE130_provenance.
- NP754787.RAf7HXKVfIHZpJCVUe5HKmjQXgXbrAW4wro_FoAU_pWDE130_assertion SIO_000772 19647026 NP754787.RAf7HXKVfIHZpJCVUe5HKmjQXgXbrAW4wro_FoAU_pWDE130_provenance.
- NP754787.RAf7HXKVfIHZpJCVUe5HKmjQXgXbrAW4wro_FoAU_pWDE130_assertion evidence source_evidence_literature NP754787.RAf7HXKVfIHZpJCVUe5HKmjQXgXbrAW4wro_FoAU_pWDE130_provenance.
- NP754787.RAf7HXKVfIHZpJCVUe5HKmjQXgXbrAW4wro_FoAU_pWDE130_assertion description "[So, HTR2A is unlikely to be a genetic marker for ASD in Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP754787.RAf7HXKVfIHZpJCVUe5HKmjQXgXbrAW4wro_FoAU_pWDE130_provenance.