Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_provenance.
- NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_provenance.
- NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_assertion evidence source_evidence_literature NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_provenance.
- NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_assertion SIO_000772 19131948 NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_provenance.
- NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_assertion wasDerivedFrom befree-20150227 NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_provenance.
- NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_assertion wasGeneratedBy ECO_0000203 NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP935228.RAYZ7Xvcp5l1U_55-yiq8Mz5EEe9DfrLZiGIAvhb8LoI0130_provenance.