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- source_evidence_literature type ECO_0000212 NP498983.RAQj6f7svDATJcruhsjOYdp401bkZFzPljLil_bzxkOao130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP498983.RAQj6f7svDATJcruhsjOYdp401bkZFzPljLil_bzxkOao130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP498983.RAQj6f7svDATJcruhsjOYdp401bkZFzPljLil_bzxkOao130_provenance.
- NP498983.RAQj6f7svDATJcruhsjOYdp401bkZFzPljLil_bzxkOao130_assertion description "[KCNQ1 is associated with two different entities of LQTS, the autosomal-dominant Romano-Ward syndrome (RWS), and the autosomal-recessive Jervell and Lange-Nielsen syndrome (JLNS) characterized by bilateral deafness in addition to cardiac arrhythmias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP498983.RAQj6f7svDATJcruhsjOYdp401bkZFzPljLil_bzxkOao130_provenance.
- NP498983.RAQj6f7svDATJcruhsjOYdp401bkZFzPljLil_bzxkOao130_assertion evidence source_evidence_literature NP498983.RAQj6f7svDATJcruhsjOYdp401bkZFzPljLil_bzxkOao130_provenance.
- NP498983.RAQj6f7svDATJcruhsjOYdp401bkZFzPljLil_bzxkOao130_assertion SIO_000772 15950200 NP498983.RAQj6f7svDATJcruhsjOYdp401bkZFzPljLil_bzxkOao130_provenance.
- NP498983.RAQj6f7svDATJcruhsjOYdp401bkZFzPljLil_bzxkOao130_assertion wasDerivedFrom befree-2016 NP498983.RAQj6f7svDATJcruhsjOYdp401bkZFzPljLil_bzxkOao130_provenance.
- NP498983.RAQj6f7svDATJcruhsjOYdp401bkZFzPljLil_bzxkOao130_assertion wasGeneratedBy ECO_0000203 NP498983.RAQj6f7svDATJcruhsjOYdp401bkZFzPljLil_bzxkOao130_provenance.
- befree-2016 importedOn "2016-02-19" NP498983.RAQj6f7svDATJcruhsjOYdp401bkZFzPljLil_bzxkOao130_provenance.