Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP691765.RA-HMz756Lh1rDXY0xM5n8EGYEKkyQVp_32Qim11HxP74130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP691765.RA-HMz756Lh1rDXY0xM5n8EGYEKkyQVp_32Qim11HxP74130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP691765.RA-HMz756Lh1rDXY0xM5n8EGYEKkyQVp_32Qim11HxP74130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP691765.RA-HMz756Lh1rDXY0xM5n8EGYEKkyQVp_32Qim11HxP74130_provenance.
- NP691765.RA-HMz756Lh1rDXY0xM5n8EGYEKkyQVp_32Qim11HxP74130_assertion wasGeneratedBy ECO_0000203 NP691765.RA-HMz756Lh1rDXY0xM5n8EGYEKkyQVp_32Qim11HxP74130_provenance.
- NP691765.RA-HMz756Lh1rDXY0xM5n8EGYEKkyQVp_32Qim11HxP74130_assertion wasDerivedFrom befree-20140225 NP691765.RA-HMz756Lh1rDXY0xM5n8EGYEKkyQVp_32Qim11HxP74130_provenance.
- NP691765.RA-HMz756Lh1rDXY0xM5n8EGYEKkyQVp_32Qim11HxP74130_assertion SIO_000772 11299060 NP691765.RA-HMz756Lh1rDXY0xM5n8EGYEKkyQVp_32Qim11HxP74130_provenance.
- NP691765.RA-HMz756Lh1rDXY0xM5n8EGYEKkyQVp_32Qim11HxP74130_assertion evidence source_evidence_literature NP691765.RA-HMz756Lh1rDXY0xM5n8EGYEKkyQVp_32Qim11HxP74130_provenance.
- NP691765.RA-HMz756Lh1rDXY0xM5n8EGYEKkyQVp_32Qim11HxP74130_assertion description "[We characterized the rearranged heavy chain variable segment (VH) genes in the SM for gene usage and the mutational pattern to elucidate the B lymphocyte involvement in AS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691765.RA-HMz756Lh1rDXY0xM5n8EGYEKkyQVp_32Qim11HxP74130_provenance.
- befree-20140225 importedOn "2014-02-25" NP691765.RA-HMz756Lh1rDXY0xM5n8EGYEKkyQVp_32Qim11HxP74130_provenance.