Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1010930.RAXOmVb_rtqrr_JV9Wg4uCDGXUGLxRUIy54WQM559URSM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1010930.RAXOmVb_rtqrr_JV9Wg4uCDGXUGLxRUIy54WQM559URSM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1010930.RAXOmVb_rtqrr_JV9Wg4uCDGXUGLxRUIy54WQM559URSM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1010930.RAXOmVb_rtqrr_JV9Wg4uCDGXUGLxRUIy54WQM559URSM130_provenance.
- NP1010930.RAXOmVb_rtqrr_JV9Wg4uCDGXUGLxRUIy54WQM559URSM130_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." NP1010930.RAXOmVb_rtqrr_JV9Wg4uCDGXUGLxRUIy54WQM559URSM130_provenance.
- NP1010930.RAXOmVb_rtqrr_JV9Wg4uCDGXUGLxRUIy54WQM559URSM130_assertion evidence source_evidence_literature NP1010930.RAXOmVb_rtqrr_JV9Wg4uCDGXUGLxRUIy54WQM559URSM130_provenance.
- NP1010930.RAXOmVb_rtqrr_JV9Wg4uCDGXUGLxRUIy54WQM559URSM130_assertion SIO_000772 21310059 NP1010930.RAXOmVb_rtqrr_JV9Wg4uCDGXUGLxRUIy54WQM559URSM130_provenance.
- NP1010930.RAXOmVb_rtqrr_JV9Wg4uCDGXUGLxRUIy54WQM559URSM130_assertion wasDerivedFrom befree-20150227 NP1010930.RAXOmVb_rtqrr_JV9Wg4uCDGXUGLxRUIy54WQM559URSM130_provenance.
- NP1010930.RAXOmVb_rtqrr_JV9Wg4uCDGXUGLxRUIy54WQM559URSM130_assertion wasGeneratedBy ECO_0000203 NP1010930.RAXOmVb_rtqrr_JV9Wg4uCDGXUGLxRUIy54WQM559URSM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1010930.RAXOmVb_rtqrr_JV9Wg4uCDGXUGLxRUIy54WQM559URSM130_provenance.