Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1045690.RAbz8xo0psX3H_jqYDlToQTuGPbHNDnb1XWpRZN8ivYgs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1045690.RAbz8xo0psX3H_jqYDlToQTuGPbHNDnb1XWpRZN8ivYgs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1045690.RAbz8xo0psX3H_jqYDlToQTuGPbHNDnb1XWpRZN8ivYgs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1045690.RAbz8xo0psX3H_jqYDlToQTuGPbHNDnb1XWpRZN8ivYgs130_provenance.
- NP1045690.RAbz8xo0psX3H_jqYDlToQTuGPbHNDnb1XWpRZN8ivYgs130_assertion description "[Maternal CVT has been associated with factor V Leiden, the prothrombin G20210A mutation, protein C deficiency and hyperhomocysteinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1045690.RAbz8xo0psX3H_jqYDlToQTuGPbHNDnb1XWpRZN8ivYgs130_provenance.
- NP1045690.RAbz8xo0psX3H_jqYDlToQTuGPbHNDnb1XWpRZN8ivYgs130_assertion evidence source_evidence_literature NP1045690.RAbz8xo0psX3H_jqYDlToQTuGPbHNDnb1XWpRZN8ivYgs130_provenance.
- NP1045690.RAbz8xo0psX3H_jqYDlToQTuGPbHNDnb1XWpRZN8ivYgs130_assertion SIO_000772 23337711 NP1045690.RAbz8xo0psX3H_jqYDlToQTuGPbHNDnb1XWpRZN8ivYgs130_provenance.
- NP1045690.RAbz8xo0psX3H_jqYDlToQTuGPbHNDnb1XWpRZN8ivYgs130_assertion wasDerivedFrom befree-2016 NP1045690.RAbz8xo0psX3H_jqYDlToQTuGPbHNDnb1XWpRZN8ivYgs130_provenance.
- NP1045690.RAbz8xo0psX3H_jqYDlToQTuGPbHNDnb1XWpRZN8ivYgs130_assertion wasGeneratedBy ECO_0000203 NP1045690.RAbz8xo0psX3H_jqYDlToQTuGPbHNDnb1XWpRZN8ivYgs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1045690.RAbz8xo0psX3H_jqYDlToQTuGPbHNDnb1XWpRZN8ivYgs130_provenance.