Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP641043.RAA-E5l_0V3PYHbL1olUBMnXPH0qSQnZIaZXyykZZ84Po130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP641043.RAA-E5l_0V3PYHbL1olUBMnXPH0qSQnZIaZXyykZZ84Po130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP641043.RAA-E5l_0V3PYHbL1olUBMnXPH0qSQnZIaZXyykZZ84Po130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP641043.RAA-E5l_0V3PYHbL1olUBMnXPH0qSQnZIaZXyykZZ84Po130_provenance.
- NP641043.RAA-E5l_0V3PYHbL1olUBMnXPH0qSQnZIaZXyykZZ84Po130_assertion description "[In newborns with homozygous protein C deficiency with very low protein C levels (1%) a purpura fulminans like syndrome was observed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP641043.RAA-E5l_0V3PYHbL1olUBMnXPH0qSQnZIaZXyykZZ84Po130_provenance.
- NP641043.RAA-E5l_0V3PYHbL1olUBMnXPH0qSQnZIaZXyykZZ84Po130_assertion evidence source_evidence_literature NP641043.RAA-E5l_0V3PYHbL1olUBMnXPH0qSQnZIaZXyykZZ84Po130_provenance.
- NP641043.RAA-E5l_0V3PYHbL1olUBMnXPH0qSQnZIaZXyykZZ84Po130_assertion SIO_000772 3524711 NP641043.RAA-E5l_0V3PYHbL1olUBMnXPH0qSQnZIaZXyykZZ84Po130_provenance.
- NP641043.RAA-E5l_0V3PYHbL1olUBMnXPH0qSQnZIaZXyykZZ84Po130_assertion wasDerivedFrom befree-20150227 NP641043.RAA-E5l_0V3PYHbL1olUBMnXPH0qSQnZIaZXyykZZ84Po130_provenance.
- NP641043.RAA-E5l_0V3PYHbL1olUBMnXPH0qSQnZIaZXyykZZ84Po130_assertion wasGeneratedBy ECO_0000203 NP641043.RAA-E5l_0V3PYHbL1olUBMnXPH0qSQnZIaZXyykZZ84Po130_provenance.
- befree-20150227 importedOn "2015-02-27" NP641043.RAA-E5l_0V3PYHbL1olUBMnXPH0qSQnZIaZXyykZZ84Po130_provenance.