Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP739017.RAWqr8wFrIyy6NnTynKjJ3Ky_H42wEmNlHWY03f5v5q7A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP739017.RAWqr8wFrIyy6NnTynKjJ3Ky_H42wEmNlHWY03f5v5q7A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP739017.RAWqr8wFrIyy6NnTynKjJ3Ky_H42wEmNlHWY03f5v5q7A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP739017.RAWqr8wFrIyy6NnTynKjJ3Ky_H42wEmNlHWY03f5v5q7A130_provenance.
- NP739017.RAWqr8wFrIyy6NnTynKjJ3Ky_H42wEmNlHWY03f5v5q7A130_assertion wasGeneratedBy ECO_0000203 NP739017.RAWqr8wFrIyy6NnTynKjJ3Ky_H42wEmNlHWY03f5v5q7A130_provenance.
- NP739017.RAWqr8wFrIyy6NnTynKjJ3Ky_H42wEmNlHWY03f5v5q7A130_assertion wasDerivedFrom befree-20140225 NP739017.RAWqr8wFrIyy6NnTynKjJ3Ky_H42wEmNlHWY03f5v5q7A130_provenance.
- NP739017.RAWqr8wFrIyy6NnTynKjJ3Ky_H42wEmNlHWY03f5v5q7A130_assertion SIO_000772 22961002 NP739017.RAWqr8wFrIyy6NnTynKjJ3Ky_H42wEmNlHWY03f5v5q7A130_provenance.
- NP739017.RAWqr8wFrIyy6NnTynKjJ3Ky_H42wEmNlHWY03f5v5q7A130_assertion evidence source_evidence_literature NP739017.RAWqr8wFrIyy6NnTynKjJ3Ky_H42wEmNlHWY03f5v5q7A130_provenance.
- NP739017.RAWqr8wFrIyy6NnTynKjJ3Ky_H42wEmNlHWY03f5v5q7A130_assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP739017.RAWqr8wFrIyy6NnTynKjJ3Ky_H42wEmNlHWY03f5v5q7A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP739017.RAWqr8wFrIyy6NnTynKjJ3Ky_H42wEmNlHWY03f5v5q7A130_provenance.