Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP673817.RAW5VUE4mqwWGKSl77Tm2ECWwSnNgR-ETXp6EKmGQIe4s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP673817.RAW5VUE4mqwWGKSl77Tm2ECWwSnNgR-ETXp6EKmGQIe4s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP673817.RAW5VUE4mqwWGKSl77Tm2ECWwSnNgR-ETXp6EKmGQIe4s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP673817.RAW5VUE4mqwWGKSl77Tm2ECWwSnNgR-ETXp6EKmGQIe4s130_provenance.
- NP673817.RAW5VUE4mqwWGKSl77Tm2ECWwSnNgR-ETXp6EKmGQIe4s130_assertion description "[Within two of these loci, DYX1C1 (15q21) and ROBO1 (3p12) have recently been proposed as dyslexia candidate genes through the molecular analysis of translocation breakpoints in dyslexic individuals carrying balanced chromosomal translocations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP673817.RAW5VUE4mqwWGKSl77Tm2ECWwSnNgR-ETXp6EKmGQIe4s130_provenance.
- NP673817.RAW5VUE4mqwWGKSl77Tm2ECWwSnNgR-ETXp6EKmGQIe4s130_assertion evidence source_evidence_literature NP673817.RAW5VUE4mqwWGKSl77Tm2ECWwSnNgR-ETXp6EKmGQIe4s130_provenance.
- NP673817.RAW5VUE4mqwWGKSl77Tm2ECWwSnNgR-ETXp6EKmGQIe4s130_assertion SIO_000772 18521840 NP673817.RAW5VUE4mqwWGKSl77Tm2ECWwSnNgR-ETXp6EKmGQIe4s130_provenance.
- NP673817.RAW5VUE4mqwWGKSl77Tm2ECWwSnNgR-ETXp6EKmGQIe4s130_assertion wasDerivedFrom befree-20150227 NP673817.RAW5VUE4mqwWGKSl77Tm2ECWwSnNgR-ETXp6EKmGQIe4s130_provenance.
- NP673817.RAW5VUE4mqwWGKSl77Tm2ECWwSnNgR-ETXp6EKmGQIe4s130_assertion wasGeneratedBy ECO_0000203 NP673817.RAW5VUE4mqwWGKSl77Tm2ECWwSnNgR-ETXp6EKmGQIe4s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP673817.RAW5VUE4mqwWGKSl77Tm2ECWwSnNgR-ETXp6EKmGQIe4s130_provenance.