Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP945917.RAPr1HgISpIY8Ph0CNuIdKj7uDE0CrEuq2Tr4ePDxMVfY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP945917.RAPr1HgISpIY8Ph0CNuIdKj7uDE0CrEuq2Tr4ePDxMVfY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP945917.RAPr1HgISpIY8Ph0CNuIdKj7uDE0CrEuq2Tr4ePDxMVfY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP945917.RAPr1HgISpIY8Ph0CNuIdKj7uDE0CrEuq2Tr4ePDxMVfY130_provenance.
- NP945917.RAPr1HgISpIY8Ph0CNuIdKj7uDE0CrEuq2Tr4ePDxMVfY130_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." NP945917.RAPr1HgISpIY8Ph0CNuIdKj7uDE0CrEuq2Tr4ePDxMVfY130_provenance.
- NP945917.RAPr1HgISpIY8Ph0CNuIdKj7uDE0CrEuq2Tr4ePDxMVfY130_assertion evidence source_evidence_literature NP945917.RAPr1HgISpIY8Ph0CNuIdKj7uDE0CrEuq2Tr4ePDxMVfY130_provenance.
- NP945917.RAPr1HgISpIY8Ph0CNuIdKj7uDE0CrEuq2Tr4ePDxMVfY130_assertion SIO_000772 22160322 NP945917.RAPr1HgISpIY8Ph0CNuIdKj7uDE0CrEuq2Tr4ePDxMVfY130_provenance.
- NP945917.RAPr1HgISpIY8Ph0CNuIdKj7uDE0CrEuq2Tr4ePDxMVfY130_assertion wasDerivedFrom befree-2016 NP945917.RAPr1HgISpIY8Ph0CNuIdKj7uDE0CrEuq2Tr4ePDxMVfY130_provenance.
- NP945917.RAPr1HgISpIY8Ph0CNuIdKj7uDE0CrEuq2Tr4ePDxMVfY130_assertion wasGeneratedBy ECO_0000203 NP945917.RAPr1HgISpIY8Ph0CNuIdKj7uDE0CrEuq2Tr4ePDxMVfY130_provenance.
- befree-2016 importedOn "2016-02-19" NP945917.RAPr1HgISpIY8Ph0CNuIdKj7uDE0CrEuq2Tr4ePDxMVfY130_provenance.