Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP189333.RABG2Cx-1qHczqnEDIZ60cjNrmoup5V96CztKy7SzweBw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP189333.RABG2Cx-1qHczqnEDIZ60cjNrmoup5V96CztKy7SzweBw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP189333.RABG2Cx-1qHczqnEDIZ60cjNrmoup5V96CztKy7SzweBw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP189333.RABG2Cx-1qHczqnEDIZ60cjNrmoup5V96CztKy7SzweBw130_provenance.
- NP189333.RABG2Cx-1qHczqnEDIZ60cjNrmoup5V96CztKy7SzweBw130_assertion description "[Identification of the genes that are mutated in genetic diseases characterized by the development of either neurofibromas and MPNSTs [neurofibromatosis type 1 (NF1)] or schwannomas [neurofibromatosis type 2 (NF2), schwannomatosis and Carney complex type 1] has greatly advanced our understanding of these mechanisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP189333.RABG2Cx-1qHczqnEDIZ60cjNrmoup5V96CztKy7SzweBw130_provenance.
- NP189333.RABG2Cx-1qHczqnEDIZ60cjNrmoup5V96CztKy7SzweBw130_assertion evidence source_evidence_literature NP189333.RABG2Cx-1qHczqnEDIZ60cjNrmoup5V96CztKy7SzweBw130_provenance.
- NP189333.RABG2Cx-1qHczqnEDIZ60cjNrmoup5V96CztKy7SzweBw130_assertion SIO_000772 22160322 NP189333.RABG2Cx-1qHczqnEDIZ60cjNrmoup5V96CztKy7SzweBw130_provenance.
- NP189333.RABG2Cx-1qHczqnEDIZ60cjNrmoup5V96CztKy7SzweBw130_assertion wasDerivedFrom befree-20140225 NP189333.RABG2Cx-1qHczqnEDIZ60cjNrmoup5V96CztKy7SzweBw130_provenance.
- NP189333.RABG2Cx-1qHczqnEDIZ60cjNrmoup5V96CztKy7SzweBw130_assertion wasGeneratedBy ECO_0000203 NP189333.RABG2Cx-1qHczqnEDIZ60cjNrmoup5V96CztKy7SzweBw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP189333.RABG2Cx-1qHczqnEDIZ60cjNrmoup5V96CztKy7SzweBw130_provenance.