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- source_evidence_literature type ECO_0000212 NP793239.RAahIB89SNNytK_lGz6f0DiTl1ecn9AarSwSOndAz3Hh8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP793239.RAahIB89SNNytK_lGz6f0DiTl1ecn9AarSwSOndAz3Hh8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP793239.RAahIB89SNNytK_lGz6f0DiTl1ecn9AarSwSOndAz3Hh8130_provenance.
- NP793239.RAahIB89SNNytK_lGz6f0DiTl1ecn9AarSwSOndAz3Hh8130_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." NP793239.RAahIB89SNNytK_lGz6f0DiTl1ecn9AarSwSOndAz3Hh8130_provenance.
- NP793239.RAahIB89SNNytK_lGz6f0DiTl1ecn9AarSwSOndAz3Hh8130_assertion evidence source_evidence_literature NP793239.RAahIB89SNNytK_lGz6f0DiTl1ecn9AarSwSOndAz3Hh8130_provenance.
- NP793239.RAahIB89SNNytK_lGz6f0DiTl1ecn9AarSwSOndAz3Hh8130_assertion SIO_000772 9801870 NP793239.RAahIB89SNNytK_lGz6f0DiTl1ecn9AarSwSOndAz3Hh8130_provenance.
- NP793239.RAahIB89SNNytK_lGz6f0DiTl1ecn9AarSwSOndAz3Hh8130_assertion wasDerivedFrom befree-20150227 NP793239.RAahIB89SNNytK_lGz6f0DiTl1ecn9AarSwSOndAz3Hh8130_provenance.
- NP793239.RAahIB89SNNytK_lGz6f0DiTl1ecn9AarSwSOndAz3Hh8130_assertion wasGeneratedBy ECO_0000203 NP793239.RAahIB89SNNytK_lGz6f0DiTl1ecn9AarSwSOndAz3Hh8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP793239.RAahIB89SNNytK_lGz6f0DiTl1ecn9AarSwSOndAz3Hh8130_provenance.