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- source_evidence_literature type ECO_0000212 NP463837.RAiRbNyr1gEzFeraAOa9r9r98nudwBIo7ClvfrkjJMUao130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP463837.RAiRbNyr1gEzFeraAOa9r9r98nudwBIo7ClvfrkjJMUao130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP463837.RAiRbNyr1gEzFeraAOa9r9r98nudwBIo7ClvfrkjJMUao130_provenance.
- NP463837.RAiRbNyr1gEzFeraAOa9r9r98nudwBIo7ClvfrkjJMUao130_assertion description "[Further, the data suggest the possibility that specific Hp polymorphisms may be associated with cGVHD development and warrant further investigation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463837.RAiRbNyr1gEzFeraAOa9r9r98nudwBIo7ClvfrkjJMUao130_provenance.
- NP463837.RAiRbNyr1gEzFeraAOa9r9r98nudwBIo7ClvfrkjJMUao130_assertion evidence source_evidence_literature NP463837.RAiRbNyr1gEzFeraAOa9r9r98nudwBIo7ClvfrkjJMUao130_provenance.
- NP463837.RAiRbNyr1gEzFeraAOa9r9r98nudwBIo7ClvfrkjJMUao130_assertion SIO_000772 19379511 NP463837.RAiRbNyr1gEzFeraAOa9r9r98nudwBIo7ClvfrkjJMUao130_provenance.
- NP463837.RAiRbNyr1gEzFeraAOa9r9r98nudwBIo7ClvfrkjJMUao130_assertion wasDerivedFrom befree-20150227 NP463837.RAiRbNyr1gEzFeraAOa9r9r98nudwBIo7ClvfrkjJMUao130_provenance.
- NP463837.RAiRbNyr1gEzFeraAOa9r9r98nudwBIo7ClvfrkjJMUao130_assertion wasGeneratedBy ECO_0000203 NP463837.RAiRbNyr1gEzFeraAOa9r9r98nudwBIo7ClvfrkjJMUao130_provenance.
- befree-20150227 importedOn "2015-02-27" NP463837.RAiRbNyr1gEzFeraAOa9r9r98nudwBIo7ClvfrkjJMUao130_provenance.