Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP220585.RAI3q0kPTLqt2LcnV7o1aaTfd6ClaSqaIOM2DkEdalrp0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP220585.RAI3q0kPTLqt2LcnV7o1aaTfd6ClaSqaIOM2DkEdalrp0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP220585.RAI3q0kPTLqt2LcnV7o1aaTfd6ClaSqaIOM2DkEdalrp0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP220585.RAI3q0kPTLqt2LcnV7o1aaTfd6ClaSqaIOM2DkEdalrp0130_provenance.
- NP220585.RAI3q0kPTLqt2LcnV7o1aaTfd6ClaSqaIOM2DkEdalrp0130_assertion wasGeneratedBy ECO_0000203 NP220585.RAI3q0kPTLqt2LcnV7o1aaTfd6ClaSqaIOM2DkEdalrp0130_provenance.
- NP220585.RAI3q0kPTLqt2LcnV7o1aaTfd6ClaSqaIOM2DkEdalrp0130_assertion wasDerivedFrom befree-20140225 NP220585.RAI3q0kPTLqt2LcnV7o1aaTfd6ClaSqaIOM2DkEdalrp0130_provenance.
- NP220585.RAI3q0kPTLqt2LcnV7o1aaTfd6ClaSqaIOM2DkEdalrp0130_assertion SIO_000772 20967465 NP220585.RAI3q0kPTLqt2LcnV7o1aaTfd6ClaSqaIOM2DkEdalrp0130_provenance.
- NP220585.RAI3q0kPTLqt2LcnV7o1aaTfd6ClaSqaIOM2DkEdalrp0130_assertion evidence source_evidence_literature NP220585.RAI3q0kPTLqt2LcnV7o1aaTfd6ClaSqaIOM2DkEdalrp0130_provenance.
- NP220585.RAI3q0kPTLqt2LcnV7o1aaTfd6ClaSqaIOM2DkEdalrp0130_assertion description "[In conclusion, we provide evidence that RAB3GAP2 mutations are not specific to Martsolf syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220585.RAI3q0kPTLqt2LcnV7o1aaTfd6ClaSqaIOM2DkEdalrp0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP220585.RAI3q0kPTLqt2LcnV7o1aaTfd6ClaSqaIOM2DkEdalrp0130_provenance.