Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP674782.RAOU_2fSM1QZK6myGPoEH97sszn-ck3LDTrb74yqqIQVw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP674782.RAOU_2fSM1QZK6myGPoEH97sszn-ck3LDTrb74yqqIQVw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674782.RAOU_2fSM1QZK6myGPoEH97sszn-ck3LDTrb74yqqIQVw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674782.RAOU_2fSM1QZK6myGPoEH97sszn-ck3LDTrb74yqqIQVw130_provenance.
- NP674782.RAOU_2fSM1QZK6myGPoEH97sszn-ck3LDTrb74yqqIQVw130_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." NP674782.RAOU_2fSM1QZK6myGPoEH97sszn-ck3LDTrb74yqqIQVw130_provenance.
- NP674782.RAOU_2fSM1QZK6myGPoEH97sszn-ck3LDTrb74yqqIQVw130_assertion evidence source_evidence_literature NP674782.RAOU_2fSM1QZK6myGPoEH97sszn-ck3LDTrb74yqqIQVw130_provenance.
- NP674782.RAOU_2fSM1QZK6myGPoEH97sszn-ck3LDTrb74yqqIQVw130_assertion SIO_000772 18521840 NP674782.RAOU_2fSM1QZK6myGPoEH97sszn-ck3LDTrb74yqqIQVw130_provenance.
- NP674782.RAOU_2fSM1QZK6myGPoEH97sszn-ck3LDTrb74yqqIQVw130_assertion wasDerivedFrom befree-2016 NP674782.RAOU_2fSM1QZK6myGPoEH97sszn-ck3LDTrb74yqqIQVw130_provenance.
- NP674782.RAOU_2fSM1QZK6myGPoEH97sszn-ck3LDTrb74yqqIQVw130_assertion wasGeneratedBy ECO_0000203 NP674782.RAOU_2fSM1QZK6myGPoEH97sszn-ck3LDTrb74yqqIQVw130_provenance.
- befree-2016 importedOn "2016-02-19" NP674782.RAOU_2fSM1QZK6myGPoEH97sszn-ck3LDTrb74yqqIQVw130_provenance.