Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615453.RA7yNNOYASFFNRWgshoXmGKXLjSDT_TKzlMoas9SHOL5Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615453.RA7yNNOYASFFNRWgshoXmGKXLjSDT_TKzlMoas9SHOL5Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615453.RA7yNNOYASFFNRWgshoXmGKXLjSDT_TKzlMoas9SHOL5Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615453.RA7yNNOYASFFNRWgshoXmGKXLjSDT_TKzlMoas9SHOL5Y130_provenance.
- NP615453.RA7yNNOYASFFNRWgshoXmGKXLjSDT_TKzlMoas9SHOL5Y130_assertion description "[Based on linkage data from the CEPH (Paris) reference families and physical mapping information from a somatic cell hybrid panel of chromosome 8 fragments, the most likely order for four of these five loci and the diseases locus is 8pter-LPL-D8S5-D8S87-PLAT-RP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615453.RA7yNNOYASFFNRWgshoXmGKXLjSDT_TKzlMoas9SHOL5Y130_provenance.
- NP615453.RA7yNNOYASFFNRWgshoXmGKXLjSDT_TKzlMoas9SHOL5Y130_assertion evidence source_evidence_literature NP615453.RA7yNNOYASFFNRWgshoXmGKXLjSDT_TKzlMoas9SHOL5Y130_provenance.
- NP615453.RA7yNNOYASFFNRWgshoXmGKXLjSDT_TKzlMoas9SHOL5Y130_assertion SIO_000772 1783394 NP615453.RA7yNNOYASFFNRWgshoXmGKXLjSDT_TKzlMoas9SHOL5Y130_provenance.
- NP615453.RA7yNNOYASFFNRWgshoXmGKXLjSDT_TKzlMoas9SHOL5Y130_assertion wasDerivedFrom befree-20140225 NP615453.RA7yNNOYASFFNRWgshoXmGKXLjSDT_TKzlMoas9SHOL5Y130_provenance.
- NP615453.RA7yNNOYASFFNRWgshoXmGKXLjSDT_TKzlMoas9SHOL5Y130_assertion wasGeneratedBy ECO_0000203 NP615453.RA7yNNOYASFFNRWgshoXmGKXLjSDT_TKzlMoas9SHOL5Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615453.RA7yNNOYASFFNRWgshoXmGKXLjSDT_TKzlMoas9SHOL5Y130_provenance.