Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP81234.RARjozuSXTjn8igrKjzEJ0SNTkG5oS9yCqZF7v6JLY1M0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP81234.RARjozuSXTjn8igrKjzEJ0SNTkG5oS9yCqZF7v6JLY1M0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP81234.RARjozuSXTjn8igrKjzEJ0SNTkG5oS9yCqZF7v6JLY1M0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP81234.RARjozuSXTjn8igrKjzEJ0SNTkG5oS9yCqZF7v6JLY1M0130_provenance.
- NP81234.RARjozuSXTjn8igrKjzEJ0SNTkG5oS9yCqZF7v6JLY1M0130_assertion description "[In SPTLC1, we detected a novel mutation (S331F) corresponding to a previously unknown severe and early-onset HSAN phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81234.RARjozuSXTjn8igrKjzEJ0SNTkG5oS9yCqZF7v6JLY1M0130_provenance.
- NP81234.RARjozuSXTjn8igrKjzEJ0SNTkG5oS9yCqZF7v6JLY1M0130_assertion evidence source_evidence_literature NP81234.RARjozuSXTjn8igrKjzEJ0SNTkG5oS9yCqZF7v6JLY1M0130_provenance.
- NP81234.RARjozuSXTjn8igrKjzEJ0SNTkG5oS9yCqZF7v6JLY1M0130_assertion SIO_000772 19651702 NP81234.RARjozuSXTjn8igrKjzEJ0SNTkG5oS9yCqZF7v6JLY1M0130_provenance.
- NP81234.RARjozuSXTjn8igrKjzEJ0SNTkG5oS9yCqZF7v6JLY1M0130_assertion wasDerivedFrom gad-20130706 NP81234.RARjozuSXTjn8igrKjzEJ0SNTkG5oS9yCqZF7v6JLY1M0130_provenance.
- NP81234.RARjozuSXTjn8igrKjzEJ0SNTkG5oS9yCqZF7v6JLY1M0130_assertion wasGeneratedBy ECO_0000203 NP81234.RARjozuSXTjn8igrKjzEJ0SNTkG5oS9yCqZF7v6JLY1M0130_provenance.
- gad-20130706 importedOn "2013-07-06" NP81234.RARjozuSXTjn8igrKjzEJ0SNTkG5oS9yCqZF7v6JLY1M0130_provenance.