Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP371987.RAd5l9zhzfbBXgznI_htVL-sSiKTP6mgCxr5esQxIblgM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP371987.RAd5l9zhzfbBXgznI_htVL-sSiKTP6mgCxr5esQxIblgM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP371987.RAd5l9zhzfbBXgznI_htVL-sSiKTP6mgCxr5esQxIblgM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP371987.RAd5l9zhzfbBXgznI_htVL-sSiKTP6mgCxr5esQxIblgM130_provenance.
- NP371987.RAd5l9zhzfbBXgznI_htVL-sSiKTP6mgCxr5esQxIblgM130_assertion description "[NPHS1 and NPHS2 gene mutations in Chinese children with sporadic nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP371987.RAd5l9zhzfbBXgznI_htVL-sSiKTP6mgCxr5esQxIblgM130_provenance.
- NP371987.RAd5l9zhzfbBXgznI_htVL-sSiKTP6mgCxr5esQxIblgM130_assertion evidence source_evidence_literature NP371987.RAd5l9zhzfbBXgznI_htVL-sSiKTP6mgCxr5esQxIblgM130_provenance.
- NP371987.RAd5l9zhzfbBXgznI_htVL-sSiKTP6mgCxr5esQxIblgM130_assertion SIO_000772 17211152 NP371987.RAd5l9zhzfbBXgznI_htVL-sSiKTP6mgCxr5esQxIblgM130_provenance.
- NP371987.RAd5l9zhzfbBXgznI_htVL-sSiKTP6mgCxr5esQxIblgM130_assertion wasDerivedFrom befree-20140225 NP371987.RAd5l9zhzfbBXgznI_htVL-sSiKTP6mgCxr5esQxIblgM130_provenance.
- NP371987.RAd5l9zhzfbBXgznI_htVL-sSiKTP6mgCxr5esQxIblgM130_assertion wasGeneratedBy ECO_0000203 NP371987.RAd5l9zhzfbBXgznI_htVL-sSiKTP6mgCxr5esQxIblgM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP371987.RAd5l9zhzfbBXgznI_htVL-sSiKTP6mgCxr5esQxIblgM130_provenance.