Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP575150.RAIgEFzwf1EE_QQOegrpTNrwERHFwxR2_BqCqMmD1Qo9I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP575150.RAIgEFzwf1EE_QQOegrpTNrwERHFwxR2_BqCqMmD1Qo9I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP575150.RAIgEFzwf1EE_QQOegrpTNrwERHFwxR2_BqCqMmD1Qo9I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP575150.RAIgEFzwf1EE_QQOegrpTNrwERHFwxR2_BqCqMmD1Qo9I130_provenance.
- NP575150.RAIgEFzwf1EE_QQOegrpTNrwERHFwxR2_BqCqMmD1Qo9I130_assertion description "[Increased RAS signaling owing to PTPN11, SOS1 and KRAS mutations causes approximately 60% of Noonan syndrome cases, and PTPN11 mutations cause 90% of LEOPARD syndrome cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575150.RAIgEFzwf1EE_QQOegrpTNrwERHFwxR2_BqCqMmD1Qo9I130_provenance.
- NP575150.RAIgEFzwf1EE_QQOegrpTNrwERHFwxR2_BqCqMmD1Qo9I130_assertion evidence source_evidence_literature NP575150.RAIgEFzwf1EE_QQOegrpTNrwERHFwxR2_BqCqMmD1Qo9I130_provenance.
- NP575150.RAIgEFzwf1EE_QQOegrpTNrwERHFwxR2_BqCqMmD1Qo9I130_assertion SIO_000772 17603483 NP575150.RAIgEFzwf1EE_QQOegrpTNrwERHFwxR2_BqCqMmD1Qo9I130_provenance.
- NP575150.RAIgEFzwf1EE_QQOegrpTNrwERHFwxR2_BqCqMmD1Qo9I130_assertion wasDerivedFrom befree-20140225 NP575150.RAIgEFzwf1EE_QQOegrpTNrwERHFwxR2_BqCqMmD1Qo9I130_provenance.
- NP575150.RAIgEFzwf1EE_QQOegrpTNrwERHFwxR2_BqCqMmD1Qo9I130_assertion wasGeneratedBy ECO_0000203 NP575150.RAIgEFzwf1EE_QQOegrpTNrwERHFwxR2_BqCqMmD1Qo9I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP575150.RAIgEFzwf1EE_QQOegrpTNrwERHFwxR2_BqCqMmD1Qo9I130_provenance.