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- source_evidence_literature type ECO_0000212 NP1383183.RAno45045s0nhZs0seEFe9-SuQWbJNgctfO6Eyd_7COkI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1383183.RAno45045s0nhZs0seEFe9-SuQWbJNgctfO6Eyd_7COkI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1383183.RAno45045s0nhZs0seEFe9-SuQWbJNgctfO6Eyd_7COkI130_provenance.
- NP1383183.RAno45045s0nhZs0seEFe9-SuQWbJNgctfO6Eyd_7COkI130_assertion description "[Previously we mapped a locus for situs abnormalities in humans, HTX1, to Xq26.2 by linkage analysis in a single family (LR1) and by detection of a deletion in an unrelated situs ambiguus male (Family LR2; refs 2,3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1383183.RAno45045s0nhZs0seEFe9-SuQWbJNgctfO6Eyd_7COkI130_provenance.
- NP1383183.RAno45045s0nhZs0seEFe9-SuQWbJNgctfO6Eyd_7COkI130_assertion evidence source_evidence_literature NP1383183.RAno45045s0nhZs0seEFe9-SuQWbJNgctfO6Eyd_7COkI130_provenance.
- NP1383183.RAno45045s0nhZs0seEFe9-SuQWbJNgctfO6Eyd_7COkI130_assertion SIO_000772 9354794 NP1383183.RAno45045s0nhZs0seEFe9-SuQWbJNgctfO6Eyd_7COkI130_provenance.
- NP1383183.RAno45045s0nhZs0seEFe9-SuQWbJNgctfO6Eyd_7COkI130_assertion wasDerivedFrom befree-2016 NP1383183.RAno45045s0nhZs0seEFe9-SuQWbJNgctfO6Eyd_7COkI130_provenance.
- NP1383183.RAno45045s0nhZs0seEFe9-SuQWbJNgctfO6Eyd_7COkI130_assertion wasGeneratedBy ECO_0000203 NP1383183.RAno45045s0nhZs0seEFe9-SuQWbJNgctfO6Eyd_7COkI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1383183.RAno45045s0nhZs0seEFe9-SuQWbJNgctfO6Eyd_7COkI130_provenance.