Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP137260.RAGa8HUdOshfbwdQNjBpDsETV9C2wjQXC_t3I6vz6k_t4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP137260.RAGa8HUdOshfbwdQNjBpDsETV9C2wjQXC_t3I6vz6k_t4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP137260.RAGa8HUdOshfbwdQNjBpDsETV9C2wjQXC_t3I6vz6k_t4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP137260.RAGa8HUdOshfbwdQNjBpDsETV9C2wjQXC_t3I6vz6k_t4130_provenance.
- NP137260.RAGa8HUdOshfbwdQNjBpDsETV9C2wjQXC_t3I6vz6k_t4130_assertion description "[In the current study, we have assigned most probable six-locus haplotypes determined by HLA-A, -Cw, -B and -DRB1 highly polymorphic genes and non-HLA LTA(+252) and TNF(-308) single nucleotide polymorphisms (SNPs) in 152 NHL Caucasian French patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP137260.RAGa8HUdOshfbwdQNjBpDsETV9C2wjQXC_t3I6vz6k_t4130_provenance.
- NP137260.RAGa8HUdOshfbwdQNjBpDsETV9C2wjQXC_t3I6vz6k_t4130_assertion evidence source_evidence_literature NP137260.RAGa8HUdOshfbwdQNjBpDsETV9C2wjQXC_t3I6vz6k_t4130_provenance.
- NP137260.RAGa8HUdOshfbwdQNjBpDsETV9C2wjQXC_t3I6vz6k_t4130_assertion SIO_000772 17971052 NP137260.RAGa8HUdOshfbwdQNjBpDsETV9C2wjQXC_t3I6vz6k_t4130_provenance.
- NP137260.RAGa8HUdOshfbwdQNjBpDsETV9C2wjQXC_t3I6vz6k_t4130_assertion wasDerivedFrom gad-20150221 NP137260.RAGa8HUdOshfbwdQNjBpDsETV9C2wjQXC_t3I6vz6k_t4130_provenance.
- NP137260.RAGa8HUdOshfbwdQNjBpDsETV9C2wjQXC_t3I6vz6k_t4130_assertion wasGeneratedBy ECO_0000203 NP137260.RAGa8HUdOshfbwdQNjBpDsETV9C2wjQXC_t3I6vz6k_t4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP137260.RAGa8HUdOshfbwdQNjBpDsETV9C2wjQXC_t3I6vz6k_t4130_provenance.