Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP691964.RAfsf3XYcXBd64RTTyVmTddmmKov3Eq4-AT7qeWFO-CUQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP691964.RAfsf3XYcXBd64RTTyVmTddmmKov3Eq4-AT7qeWFO-CUQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP691964.RAfsf3XYcXBd64RTTyVmTddmmKov3Eq4-AT7qeWFO-CUQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP691964.RAfsf3XYcXBd64RTTyVmTddmmKov3Eq4-AT7qeWFO-CUQ130_provenance.
- NP691964.RAfsf3XYcXBd64RTTyVmTddmmKov3Eq4-AT7qeWFO-CUQ130_assertion description "[Our study indicates that missense single nucleotide polymorphisms and haplotypes of SFTPA1, SFTPA2 and SFTPD are associated with susceptibility to CAP, and that several haplotypes also influence severity and outcome of CAP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691964.RAfsf3XYcXBd64RTTyVmTddmmKov3Eq4-AT7qeWFO-CUQ130_provenance.
- NP691964.RAfsf3XYcXBd64RTTyVmTddmmKov3Eq4-AT7qeWFO-CUQ130_assertion evidence source_evidence_literature NP691964.RAfsf3XYcXBd64RTTyVmTddmmKov3Eq4-AT7qeWFO-CUQ130_provenance.
- NP691964.RAfsf3XYcXBd64RTTyVmTddmmKov3Eq4-AT7qeWFO-CUQ130_assertion SIO_000772 21310059 NP691964.RAfsf3XYcXBd64RTTyVmTddmmKov3Eq4-AT7qeWFO-CUQ130_provenance.
- NP691964.RAfsf3XYcXBd64RTTyVmTddmmKov3Eq4-AT7qeWFO-CUQ130_assertion wasDerivedFrom befree-20150227 NP691964.RAfsf3XYcXBd64RTTyVmTddmmKov3Eq4-AT7qeWFO-CUQ130_provenance.
- NP691964.RAfsf3XYcXBd64RTTyVmTddmmKov3Eq4-AT7qeWFO-CUQ130_assertion wasGeneratedBy ECO_0000203 NP691964.RAfsf3XYcXBd64RTTyVmTddmmKov3Eq4-AT7qeWFO-CUQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP691964.RAfsf3XYcXBd64RTTyVmTddmmKov3Eq4-AT7qeWFO-CUQ130_provenance.