Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP286722.RA2X1kjTbDuE0PNJ90KzeJm58VQdnR9fvE3lf6D9sZfc0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP286722.RA2X1kjTbDuE0PNJ90KzeJm58VQdnR9fvE3lf6D9sZfc0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP286722.RA2X1kjTbDuE0PNJ90KzeJm58VQdnR9fvE3lf6D9sZfc0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP286722.RA2X1kjTbDuE0PNJ90KzeJm58VQdnR9fvE3lf6D9sZfc0130_provenance.
- NP286722.RA2X1kjTbDuE0PNJ90KzeJm58VQdnR9fvE3lf6D9sZfc0130_assertion wasGeneratedBy ECO_0000203 NP286722.RA2X1kjTbDuE0PNJ90KzeJm58VQdnR9fvE3lf6D9sZfc0130_provenance.
- NP286722.RA2X1kjTbDuE0PNJ90KzeJm58VQdnR9fvE3lf6D9sZfc0130_assertion wasDerivedFrom befree-20140225 NP286722.RA2X1kjTbDuE0PNJ90KzeJm58VQdnR9fvE3lf6D9sZfc0130_provenance.
- NP286722.RA2X1kjTbDuE0PNJ90KzeJm58VQdnR9fvE3lf6D9sZfc0130_assertion SIO_000772 9833609 NP286722.RA2X1kjTbDuE0PNJ90KzeJm58VQdnR9fvE3lf6D9sZfc0130_provenance.
- NP286722.RA2X1kjTbDuE0PNJ90KzeJm58VQdnR9fvE3lf6D9sZfc0130_assertion evidence source_evidence_literature NP286722.RA2X1kjTbDuE0PNJ90KzeJm58VQdnR9fvE3lf6D9sZfc0130_provenance.
- NP286722.RA2X1kjTbDuE0PNJ90KzeJm58VQdnR9fvE3lf6D9sZfc0130_assertion description "[Among these, IGF2 and H19 tightly linked on human chromosome 11 are of special interest because of their reciprocal imprinting and possible association with certain malignancy and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP286722.RA2X1kjTbDuE0PNJ90KzeJm58VQdnR9fvE3lf6D9sZfc0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP286722.RA2X1kjTbDuE0PNJ90KzeJm58VQdnR9fvE3lf6D9sZfc0130_provenance.