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- source_evidence_literature type ECO_0000212 NP570265.RAa9avD6En2JY8lQydJ8HXd-T9-dHPa1rj8O3Z_gdP2l4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP570265.RAa9avD6En2JY8lQydJ8HXd-T9-dHPa1rj8O3Z_gdP2l4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP570265.RAa9avD6En2JY8lQydJ8HXd-T9-dHPa1rj8O3Z_gdP2l4130_provenance.
- NP570265.RAa9avD6En2JY8lQydJ8HXd-T9-dHPa1rj8O3Z_gdP2l4130_assertion description "[Direct evidence for MSH2 abnormalities in human LBL was established by sequence analysis of exon 13 of hMSH2, which revealed coding region mutations in 2 of 10 cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570265.RAa9avD6En2JY8lQydJ8HXd-T9-dHPa1rj8O3Z_gdP2l4130_provenance.
- NP570265.RAa9avD6En2JY8lQydJ8HXd-T9-dHPa1rj8O3Z_gdP2l4130_assertion evidence source_evidence_literature NP570265.RAa9avD6En2JY8lQydJ8HXd-T9-dHPa1rj8O3Z_gdP2l4130_provenance.
- NP570265.RAa9avD6En2JY8lQydJ8HXd-T9-dHPa1rj8O3Z_gdP2l4130_assertion SIO_000772 9116269 NP570265.RAa9avD6En2JY8lQydJ8HXd-T9-dHPa1rj8O3Z_gdP2l4130_provenance.
- NP570265.RAa9avD6En2JY8lQydJ8HXd-T9-dHPa1rj8O3Z_gdP2l4130_assertion wasDerivedFrom befree-20150227 NP570265.RAa9avD6En2JY8lQydJ8HXd-T9-dHPa1rj8O3Z_gdP2l4130_provenance.
- NP570265.RAa9avD6En2JY8lQydJ8HXd-T9-dHPa1rj8O3Z_gdP2l4130_assertion wasGeneratedBy ECO_0000203 NP570265.RAa9avD6En2JY8lQydJ8HXd-T9-dHPa1rj8O3Z_gdP2l4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP570265.RAa9avD6En2JY8lQydJ8HXd-T9-dHPa1rj8O3Z_gdP2l4130_provenance.