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- source_evidence_literature type ECO_0000212 NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_provenance.
- NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_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." NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_provenance.
- NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_assertion evidence source_evidence_literature NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_provenance.
- NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_assertion SIO_000772 18521840 NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_provenance.
- NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_assertion wasDerivedFrom befree-20150227 NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_provenance.
- NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_assertion wasGeneratedBy ECO_0000203 NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_provenance.