Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1249006.RAMKC2qx4bZPqsZH0yYUp7UbrGUiRQasQS7jG2FIZNmLA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1249006.RAMKC2qx4bZPqsZH0yYUp7UbrGUiRQasQS7jG2FIZNmLA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1249006.RAMKC2qx4bZPqsZH0yYUp7UbrGUiRQasQS7jG2FIZNmLA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1249006.RAMKC2qx4bZPqsZH0yYUp7UbrGUiRQasQS7jG2FIZNmLA130_provenance.
- NP1249006.RAMKC2qx4bZPqsZH0yYUp7UbrGUiRQasQS7jG2FIZNmLA130_assertion description "[Thus, the number of HLA-A, -B, -C, -DPB1, and DRB1_DQB1 mismatches showed a clear-cut risk difference for acute GVHD, whereas the number of mismatches for HLA-A, -B, -C, and DRB1_DQB1 showed the same for mortality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249006.RAMKC2qx4bZPqsZH0yYUp7UbrGUiRQasQS7jG2FIZNmLA130_provenance.
- NP1249006.RAMKC2qx4bZPqsZH0yYUp7UbrGUiRQasQS7jG2FIZNmLA130_assertion evidence source_evidence_literature NP1249006.RAMKC2qx4bZPqsZH0yYUp7UbrGUiRQasQS7jG2FIZNmLA130_provenance.
- NP1249006.RAMKC2qx4bZPqsZH0yYUp7UbrGUiRQasQS7jG2FIZNmLA130_assertion SIO_000772 25519752 NP1249006.RAMKC2qx4bZPqsZH0yYUp7UbrGUiRQasQS7jG2FIZNmLA130_provenance.
- NP1249006.RAMKC2qx4bZPqsZH0yYUp7UbrGUiRQasQS7jG2FIZNmLA130_assertion wasDerivedFrom befree-2016 NP1249006.RAMKC2qx4bZPqsZH0yYUp7UbrGUiRQasQS7jG2FIZNmLA130_provenance.
- NP1249006.RAMKC2qx4bZPqsZH0yYUp7UbrGUiRQasQS7jG2FIZNmLA130_assertion wasGeneratedBy ECO_0000203 NP1249006.RAMKC2qx4bZPqsZH0yYUp7UbrGUiRQasQS7jG2FIZNmLA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1249006.RAMKC2qx4bZPqsZH0yYUp7UbrGUiRQasQS7jG2FIZNmLA130_provenance.