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- source_evidence_literature type ECO_0000212 NP877775.RA7_I37-AHIPDNT5qXsBPSf3Xw-y0lon8_ASr5L92_7_U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP877775.RA7_I37-AHIPDNT5qXsBPSf3Xw-y0lon8_ASr5L92_7_U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP877775.RA7_I37-AHIPDNT5qXsBPSf3Xw-y0lon8_ASr5L92_7_U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP877775.RA7_I37-AHIPDNT5qXsBPSf3Xw-y0lon8_ASr5L92_7_U130_provenance.
- NP877775.RA7_I37-AHIPDNT5qXsBPSf3Xw-y0lon8_ASr5L92_7_U130_assertion wasGeneratedBy ECO_0000203 NP877775.RA7_I37-AHIPDNT5qXsBPSf3Xw-y0lon8_ASr5L92_7_U130_provenance.
- NP877775.RA7_I37-AHIPDNT5qXsBPSf3Xw-y0lon8_ASr5L92_7_U130_assertion wasDerivedFrom befree-20150227 NP877775.RA7_I37-AHIPDNT5qXsBPSf3Xw-y0lon8_ASr5L92_7_U130_provenance.
- NP877775.RA7_I37-AHIPDNT5qXsBPSf3Xw-y0lon8_ASr5L92_7_U130_assertion SIO_000772 20967465 NP877775.RA7_I37-AHIPDNT5qXsBPSf3Xw-y0lon8_ASr5L92_7_U130_provenance.
- NP877775.RA7_I37-AHIPDNT5qXsBPSf3Xw-y0lon8_ASr5L92_7_U130_assertion evidence source_evidence_literature NP877775.RA7_I37-AHIPDNT5qXsBPSf3Xw-y0lon8_ASr5L92_7_U130_provenance.
- NP877775.RA7_I37-AHIPDNT5qXsBPSf3Xw-y0lon8_ASr5L92_7_U130_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." NP877775.RA7_I37-AHIPDNT5qXsBPSf3Xw-y0lon8_ASr5L92_7_U130_provenance.