Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP715603.RArr2m5vOxpoR7O80aQ95DBsKvAvWx5lOJdLLbojMVr_0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP715603.RArr2m5vOxpoR7O80aQ95DBsKvAvWx5lOJdLLbojMVr_0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP715603.RArr2m5vOxpoR7O80aQ95DBsKvAvWx5lOJdLLbojMVr_0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP715603.RArr2m5vOxpoR7O80aQ95DBsKvAvWx5lOJdLLbojMVr_0130_provenance.
- NP715603.RArr2m5vOxpoR7O80aQ95DBsKvAvWx5lOJdLLbojMVr_0130_assertion description "[Mutational analysis of the affected MEK1 and MEK2 exons did not reveal occurrence of mutations among 75 patients with Noonan syndrome, confirming the low prevalence of MEK gene defects in this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715603.RArr2m5vOxpoR7O80aQ95DBsKvAvWx5lOJdLLbojMVr_0130_provenance.
- NP715603.RArr2m5vOxpoR7O80aQ95DBsKvAvWx5lOJdLLbojMVr_0130_assertion evidence source_evidence_literature NP715603.RArr2m5vOxpoR7O80aQ95DBsKvAvWx5lOJdLLbojMVr_0130_provenance.
- NP715603.RArr2m5vOxpoR7O80aQ95DBsKvAvWx5lOJdLLbojMVr_0130_assertion SIO_000772 19156172 NP715603.RArr2m5vOxpoR7O80aQ95DBsKvAvWx5lOJdLLbojMVr_0130_provenance.
- NP715603.RArr2m5vOxpoR7O80aQ95DBsKvAvWx5lOJdLLbojMVr_0130_assertion wasDerivedFrom befree-2016 NP715603.RArr2m5vOxpoR7O80aQ95DBsKvAvWx5lOJdLLbojMVr_0130_provenance.
- NP715603.RArr2m5vOxpoR7O80aQ95DBsKvAvWx5lOJdLLbojMVr_0130_assertion wasGeneratedBy ECO_0000203 NP715603.RArr2m5vOxpoR7O80aQ95DBsKvAvWx5lOJdLLbojMVr_0130_provenance.
- befree-2016 importedOn "2016-02-19" NP715603.RArr2m5vOxpoR7O80aQ95DBsKvAvWx5lOJdLLbojMVr_0130_provenance.