Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP793241.RA1ZkhiqB_7xoa4p-fzG4L2oDN_zCbGyU88cRIX-jrc0g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP793241.RA1ZkhiqB_7xoa4p-fzG4L2oDN_zCbGyU88cRIX-jrc0g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP793241.RA1ZkhiqB_7xoa4p-fzG4L2oDN_zCbGyU88cRIX-jrc0g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP793241.RA1ZkhiqB_7xoa4p-fzG4L2oDN_zCbGyU88cRIX-jrc0g130_provenance.
- NP793241.RA1ZkhiqB_7xoa4p-fzG4L2oDN_zCbGyU88cRIX-jrc0g130_assertion description "[We used fine mapping techniques to localise UHX1 between markers DXS1266 and DXS337, where congenital stationary night blindness (XICSNB) and retinitis pigmentosa type 2 (RP2) are also located.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP793241.RA1ZkhiqB_7xoa4p-fzG4L2oDN_zCbGyU88cRIX-jrc0g130_provenance.
- NP793241.RA1ZkhiqB_7xoa4p-fzG4L2oDN_zCbGyU88cRIX-jrc0g130_assertion evidence source_evidence_literature NP793241.RA1ZkhiqB_7xoa4p-fzG4L2oDN_zCbGyU88cRIX-jrc0g130_provenance.
- NP793241.RA1ZkhiqB_7xoa4p-fzG4L2oDN_zCbGyU88cRIX-jrc0g130_assertion SIO_000772 9801870 NP793241.RA1ZkhiqB_7xoa4p-fzG4L2oDN_zCbGyU88cRIX-jrc0g130_provenance.
- NP793241.RA1ZkhiqB_7xoa4p-fzG4L2oDN_zCbGyU88cRIX-jrc0g130_assertion wasDerivedFrom befree-20150227 NP793241.RA1ZkhiqB_7xoa4p-fzG4L2oDN_zCbGyU88cRIX-jrc0g130_provenance.
- NP793241.RA1ZkhiqB_7xoa4p-fzG4L2oDN_zCbGyU88cRIX-jrc0g130_assertion wasGeneratedBy ECO_0000203 NP793241.RA1ZkhiqB_7xoa4p-fzG4L2oDN_zCbGyU88cRIX-jrc0g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP793241.RA1ZkhiqB_7xoa4p-fzG4L2oDN_zCbGyU88cRIX-jrc0g130_provenance.