Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP108362.RAOW7CHyg4C3KI9yWo8gxbh_wlt2--U7rJzlgYFvAR0SQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP108362.RAOW7CHyg4C3KI9yWo8gxbh_wlt2--U7rJzlgYFvAR0SQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP108362.RAOW7CHyg4C3KI9yWo8gxbh_wlt2--U7rJzlgYFvAR0SQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP108362.RAOW7CHyg4C3KI9yWo8gxbh_wlt2--U7rJzlgYFvAR0SQ130_provenance.
- NP108362.RAOW7CHyg4C3KI9yWo8gxbh_wlt2--U7rJzlgYFvAR0SQ130_assertion description "[PC deficiency was frequent in pediatric PVT patients and does not seem to be an inherited condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP108362.RAOW7CHyg4C3KI9yWo8gxbh_wlt2--U7rJzlgYFvAR0SQ130_provenance.
- NP108362.RAOW7CHyg4C3KI9yWo8gxbh_wlt2--U7rJzlgYFvAR0SQ130_assertion evidence source_evidence_literature NP108362.RAOW7CHyg4C3KI9yWo8gxbh_wlt2--U7rJzlgYFvAR0SQ130_provenance.
- NP108362.RAOW7CHyg4C3KI9yWo8gxbh_wlt2--U7rJzlgYFvAR0SQ130_assertion SIO_000772 15359390 NP108362.RAOW7CHyg4C3KI9yWo8gxbh_wlt2--U7rJzlgYFvAR0SQ130_provenance.
- NP108362.RAOW7CHyg4C3KI9yWo8gxbh_wlt2--U7rJzlgYFvAR0SQ130_assertion wasDerivedFrom gad-20150221 NP108362.RAOW7CHyg4C3KI9yWo8gxbh_wlt2--U7rJzlgYFvAR0SQ130_provenance.
- NP108362.RAOW7CHyg4C3KI9yWo8gxbh_wlt2--U7rJzlgYFvAR0SQ130_assertion wasGeneratedBy ECO_0000203 NP108362.RAOW7CHyg4C3KI9yWo8gxbh_wlt2--U7rJzlgYFvAR0SQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP108362.RAOW7CHyg4C3KI9yWo8gxbh_wlt2--U7rJzlgYFvAR0SQ130_provenance.