Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP159117.RAUktnmDpGkBDq0fX_x9ydWxYGxbnLvDCEMgaOmrpU2lE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP159117.RAUktnmDpGkBDq0fX_x9ydWxYGxbnLvDCEMgaOmrpU2lE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP159117.RAUktnmDpGkBDq0fX_x9ydWxYGxbnLvDCEMgaOmrpU2lE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP159117.RAUktnmDpGkBDq0fX_x9ydWxYGxbnLvDCEMgaOmrpU2lE130_provenance.
- NP159117.RAUktnmDpGkBDq0fX_x9ydWxYGxbnLvDCEMgaOmrpU2lE130_assertion description "[In addition, a polymorphic dinucleotide repeat marker located within the PAX2 gene segregated independently of the disease trait in one large family who primarily had VUR or reflux nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP159117.RAUktnmDpGkBDq0fX_x9ydWxYGxbnLvDCEMgaOmrpU2lE130_provenance.
- NP159117.RAUktnmDpGkBDq0fX_x9ydWxYGxbnLvDCEMgaOmrpU2lE130_assertion evidence source_evidence_literature NP159117.RAUktnmDpGkBDq0fX_x9ydWxYGxbnLvDCEMgaOmrpU2lE130_provenance.
- NP159117.RAUktnmDpGkBDq0fX_x9ydWxYGxbnLvDCEMgaOmrpU2lE130_assertion SIO_000772 9598733 NP159117.RAUktnmDpGkBDq0fX_x9ydWxYGxbnLvDCEMgaOmrpU2lE130_provenance.
- NP159117.RAUktnmDpGkBDq0fX_x9ydWxYGxbnLvDCEMgaOmrpU2lE130_assertion wasDerivedFrom befree-20140225 NP159117.RAUktnmDpGkBDq0fX_x9ydWxYGxbnLvDCEMgaOmrpU2lE130_provenance.
- NP159117.RAUktnmDpGkBDq0fX_x9ydWxYGxbnLvDCEMgaOmrpU2lE130_assertion wasGeneratedBy ECO_0000203 NP159117.RAUktnmDpGkBDq0fX_x9ydWxYGxbnLvDCEMgaOmrpU2lE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP159117.RAUktnmDpGkBDq0fX_x9ydWxYGxbnLvDCEMgaOmrpU2lE130_provenance.