Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP428357.RAYFJNvXGhJvrt0M8w0e6sj1DHSjVsCxepOWlcV9-FiKc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP428357.RAYFJNvXGhJvrt0M8w0e6sj1DHSjVsCxepOWlcV9-FiKc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP428357.RAYFJNvXGhJvrt0M8w0e6sj1DHSjVsCxepOWlcV9-FiKc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP428357.RAYFJNvXGhJvrt0M8w0e6sj1DHSjVsCxepOWlcV9-FiKc130_provenance.
- NP428357.RAYFJNvXGhJvrt0M8w0e6sj1DHSjVsCxepOWlcV9-FiKc130_assertion description "[According to present knowledge, congenital bilateral absence of vas deferens (CBAVD), acute recurrent or chronic pancreatitis and disseminated bronchiectasis, all with CFTR dysfunction, are CFTR-RDs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428357.RAYFJNvXGhJvrt0M8w0e6sj1DHSjVsCxepOWlcV9-FiKc130_provenance.
- NP428357.RAYFJNvXGhJvrt0M8w0e6sj1DHSjVsCxepOWlcV9-FiKc130_assertion evidence source_evidence_literature NP428357.RAYFJNvXGhJvrt0M8w0e6sj1DHSjVsCxepOWlcV9-FiKc130_provenance.
- NP428357.RAYFJNvXGhJvrt0M8w0e6sj1DHSjVsCxepOWlcV9-FiKc130_assertion SIO_000772 21658649 NP428357.RAYFJNvXGhJvrt0M8w0e6sj1DHSjVsCxepOWlcV9-FiKc130_provenance.
- NP428357.RAYFJNvXGhJvrt0M8w0e6sj1DHSjVsCxepOWlcV9-FiKc130_assertion wasDerivedFrom befree-20140225 NP428357.RAYFJNvXGhJvrt0M8w0e6sj1DHSjVsCxepOWlcV9-FiKc130_provenance.
- NP428357.RAYFJNvXGhJvrt0M8w0e6sj1DHSjVsCxepOWlcV9-FiKc130_assertion wasGeneratedBy ECO_0000203 NP428357.RAYFJNvXGhJvrt0M8w0e6sj1DHSjVsCxepOWlcV9-FiKc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP428357.RAYFJNvXGhJvrt0M8w0e6sj1DHSjVsCxepOWlcV9-FiKc130_provenance.