Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP251841.RAtjaWbWi7ZqwH8vZXpq4BhOE59KAyHNszg1Jw8QVc_HA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP251841.RAtjaWbWi7ZqwH8vZXpq4BhOE59KAyHNszg1Jw8QVc_HA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP251841.RAtjaWbWi7ZqwH8vZXpq4BhOE59KAyHNszg1Jw8QVc_HA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP251841.RAtjaWbWi7ZqwH8vZXpq4BhOE59KAyHNszg1Jw8QVc_HA130_provenance.
- NP251841.RAtjaWbWi7ZqwH8vZXpq4BhOE59KAyHNszg1Jw8QVc_HA130_assertion description "[Our observations suggest that SMAP1 loss-of-function mutations in MSI CRC may contribute to the emerging oncogenic pathway involving abnormal Arf6 regulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251841.RAtjaWbWi7ZqwH8vZXpq4BhOE59KAyHNszg1Jw8QVc_HA130_provenance.
- NP251841.RAtjaWbWi7ZqwH8vZXpq4BhOE59KAyHNszg1Jw8QVc_HA130_assertion evidence source_evidence_literature NP251841.RAtjaWbWi7ZqwH8vZXpq4BhOE59KAyHNszg1Jw8QVc_HA130_provenance.
- NP251841.RAtjaWbWi7ZqwH8vZXpq4BhOE59KAyHNszg1Jw8QVc_HA130_assertion SIO_000772 23752192 NP251841.RAtjaWbWi7ZqwH8vZXpq4BhOE59KAyHNszg1Jw8QVc_HA130_provenance.
- NP251841.RAtjaWbWi7ZqwH8vZXpq4BhOE59KAyHNszg1Jw8QVc_HA130_assertion wasDerivedFrom befree-20150227 NP251841.RAtjaWbWi7ZqwH8vZXpq4BhOE59KAyHNszg1Jw8QVc_HA130_provenance.
- NP251841.RAtjaWbWi7ZqwH8vZXpq4BhOE59KAyHNszg1Jw8QVc_HA130_assertion wasGeneratedBy ECO_0000203 NP251841.RAtjaWbWi7ZqwH8vZXpq4BhOE59KAyHNszg1Jw8QVc_HA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP251841.RAtjaWbWi7ZqwH8vZXpq4BhOE59KAyHNszg1Jw8QVc_HA130_provenance.