Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP846015.RAL3wMjDA3wz3ha4NF3aJNeidlSJXSGeKC6Tetmpl_sYE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP846015.RAL3wMjDA3wz3ha4NF3aJNeidlSJXSGeKC6Tetmpl_sYE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP846015.RAL3wMjDA3wz3ha4NF3aJNeidlSJXSGeKC6Tetmpl_sYE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP846015.RAL3wMjDA3wz3ha4NF3aJNeidlSJXSGeKC6Tetmpl_sYE130_provenance.
- NP846015.RAL3wMjDA3wz3ha4NF3aJNeidlSJXSGeKC6Tetmpl_sYE130_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." NP846015.RAL3wMjDA3wz3ha4NF3aJNeidlSJXSGeKC6Tetmpl_sYE130_provenance.
- NP846015.RAL3wMjDA3wz3ha4NF3aJNeidlSJXSGeKC6Tetmpl_sYE130_assertion evidence source_evidence_literature NP846015.RAL3wMjDA3wz3ha4NF3aJNeidlSJXSGeKC6Tetmpl_sYE130_provenance.
- NP846015.RAL3wMjDA3wz3ha4NF3aJNeidlSJXSGeKC6Tetmpl_sYE130_assertion SIO_000772 9801870 NP846015.RAL3wMjDA3wz3ha4NF3aJNeidlSJXSGeKC6Tetmpl_sYE130_provenance.
- NP846015.RAL3wMjDA3wz3ha4NF3aJNeidlSJXSGeKC6Tetmpl_sYE130_assertion wasDerivedFrom befree-20140225 NP846015.RAL3wMjDA3wz3ha4NF3aJNeidlSJXSGeKC6Tetmpl_sYE130_provenance.
- NP846015.RAL3wMjDA3wz3ha4NF3aJNeidlSJXSGeKC6Tetmpl_sYE130_assertion wasGeneratedBy ECO_0000203 NP846015.RAL3wMjDA3wz3ha4NF3aJNeidlSJXSGeKC6Tetmpl_sYE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP846015.RAL3wMjDA3wz3ha4NF3aJNeidlSJXSGeKC6Tetmpl_sYE130_provenance.