Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP600121.RAGxfHXmnFomVGoYMhnobIIDhV99yLbfll-vJwb09E6So130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP600121.RAGxfHXmnFomVGoYMhnobIIDhV99yLbfll-vJwb09E6So130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP600121.RAGxfHXmnFomVGoYMhnobIIDhV99yLbfll-vJwb09E6So130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP600121.RAGxfHXmnFomVGoYMhnobIIDhV99yLbfll-vJwb09E6So130_provenance.
- NP600121.RAGxfHXmnFomVGoYMhnobIIDhV99yLbfll-vJwb09E6So130_assertion description "[The phenotypic overlap was explained by the involvement of the Ras pathway in both disorders, and, accordingly, clustering of the NF1 mutations in the GTPase-activating protein (GAP) domain of neurofibromin was observed in individuals with NFNS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600121.RAGxfHXmnFomVGoYMhnobIIDhV99yLbfll-vJwb09E6So130_provenance.
- NP600121.RAGxfHXmnFomVGoYMhnobIIDhV99yLbfll-vJwb09E6So130_assertion evidence source_evidence_literature NP600121.RAGxfHXmnFomVGoYMhnobIIDhV99yLbfll-vJwb09E6So130_provenance.
- NP600121.RAGxfHXmnFomVGoYMhnobIIDhV99yLbfll-vJwb09E6So130_assertion SIO_000772 19449407 NP600121.RAGxfHXmnFomVGoYMhnobIIDhV99yLbfll-vJwb09E6So130_provenance.
- NP600121.RAGxfHXmnFomVGoYMhnobIIDhV99yLbfll-vJwb09E6So130_assertion wasDerivedFrom befree-20140225 NP600121.RAGxfHXmnFomVGoYMhnobIIDhV99yLbfll-vJwb09E6So130_provenance.
- NP600121.RAGxfHXmnFomVGoYMhnobIIDhV99yLbfll-vJwb09E6So130_assertion wasGeneratedBy ECO_0000203 NP600121.RAGxfHXmnFomVGoYMhnobIIDhV99yLbfll-vJwb09E6So130_provenance.
- befree-20140225 importedOn "2014-02-25" NP600121.RAGxfHXmnFomVGoYMhnobIIDhV99yLbfll-vJwb09E6So130_provenance.