Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1405230.RAoVAEx4c0eZhAl3xbSAbCyaul0C1iI0fqREsmMpiUr5s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1405230.RAoVAEx4c0eZhAl3xbSAbCyaul0C1iI0fqREsmMpiUr5s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1405230.RAoVAEx4c0eZhAl3xbSAbCyaul0C1iI0fqREsmMpiUr5s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1405230.RAoVAEx4c0eZhAl3xbSAbCyaul0C1iI0fqREsmMpiUr5s130_provenance.
- NP1405230.RAoVAEx4c0eZhAl3xbSAbCyaul0C1iI0fqREsmMpiUr5s130_assertion description "[There is a significant overlap in PC antigen and functional levels between heterozygotes of PC deficiency and normals leaving a gray zone of uncertainty in differentiating congenital PC deficiency and normal individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1405230.RAoVAEx4c0eZhAl3xbSAbCyaul0C1iI0fqREsmMpiUr5s130_provenance.
- NP1405230.RAoVAEx4c0eZhAl3xbSAbCyaul0C1iI0fqREsmMpiUr5s130_assertion evidence source_evidence_literature NP1405230.RAoVAEx4c0eZhAl3xbSAbCyaul0C1iI0fqREsmMpiUr5s130_provenance.
- NP1405230.RAoVAEx4c0eZhAl3xbSAbCyaul0C1iI0fqREsmMpiUr5s130_assertion SIO_000772 9763348 NP1405230.RAoVAEx4c0eZhAl3xbSAbCyaul0C1iI0fqREsmMpiUr5s130_provenance.
- NP1405230.RAoVAEx4c0eZhAl3xbSAbCyaul0C1iI0fqREsmMpiUr5s130_assertion wasDerivedFrom befree-2016 NP1405230.RAoVAEx4c0eZhAl3xbSAbCyaul0C1iI0fqREsmMpiUr5s130_provenance.
- NP1405230.RAoVAEx4c0eZhAl3xbSAbCyaul0C1iI0fqREsmMpiUr5s130_assertion wasGeneratedBy ECO_0000203 NP1405230.RAoVAEx4c0eZhAl3xbSAbCyaul0C1iI0fqREsmMpiUr5s130_provenance.
- befree-2016 importedOn "2016-02-19" NP1405230.RAoVAEx4c0eZhAl3xbSAbCyaul0C1iI0fqREsmMpiUr5s130_provenance.