Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP694765.RAlNNizTMqwssM-mwSGNasnAtErkK-i13MNuTw_uXWPQY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP694765.RAlNNizTMqwssM-mwSGNasnAtErkK-i13MNuTw_uXWPQY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694765.RAlNNizTMqwssM-mwSGNasnAtErkK-i13MNuTw_uXWPQY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694765.RAlNNizTMqwssM-mwSGNasnAtErkK-i13MNuTw_uXWPQY130_provenance.
- NP694765.RAlNNizTMqwssM-mwSGNasnAtErkK-i13MNuTw_uXWPQY130_assertion description "[Six1 is a crucial regulator of renal development: mutations in human SIX1 cause branchio-oto-renal (BOR) syndrome and Six1(-/-) mice exhibit renal agenesis, although the ureter is present.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694765.RAlNNizTMqwssM-mwSGNasnAtErkK-i13MNuTw_uXWPQY130_provenance.
- NP694765.RAlNNizTMqwssM-mwSGNasnAtErkK-i13MNuTw_uXWPQY130_assertion evidence source_evidence_literature NP694765.RAlNNizTMqwssM-mwSGNasnAtErkK-i13MNuTw_uXWPQY130_provenance.
- NP694765.RAlNNizTMqwssM-mwSGNasnAtErkK-i13MNuTw_uXWPQY130_assertion SIO_000772 20110314 NP694765.RAlNNizTMqwssM-mwSGNasnAtErkK-i13MNuTw_uXWPQY130_provenance.
- NP694765.RAlNNizTMqwssM-mwSGNasnAtErkK-i13MNuTw_uXWPQY130_assertion wasDerivedFrom befree-20150227 NP694765.RAlNNizTMqwssM-mwSGNasnAtErkK-i13MNuTw_uXWPQY130_provenance.
- NP694765.RAlNNizTMqwssM-mwSGNasnAtErkK-i13MNuTw_uXWPQY130_assertion wasGeneratedBy ECO_0000203 NP694765.RAlNNizTMqwssM-mwSGNasnAtErkK-i13MNuTw_uXWPQY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP694765.RAlNNizTMqwssM-mwSGNasnAtErkK-i13MNuTw_uXWPQY130_provenance.