Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP908271.RA7mzPLroip5Iww5VnSwTyiQXYlzfVOu69jh3gKp7LuD4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP908271.RA7mzPLroip5Iww5VnSwTyiQXYlzfVOu69jh3gKp7LuD4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP908271.RA7mzPLroip5Iww5VnSwTyiQXYlzfVOu69jh3gKp7LuD4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP908271.RA7mzPLroip5Iww5VnSwTyiQXYlzfVOu69jh3gKp7LuD4130_provenance.
- NP908271.RA7mzPLroip5Iww5VnSwTyiQXYlzfVOu69jh3gKp7LuD4130_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." NP908271.RA7mzPLroip5Iww5VnSwTyiQXYlzfVOu69jh3gKp7LuD4130_provenance.
- NP908271.RA7mzPLroip5Iww5VnSwTyiQXYlzfVOu69jh3gKp7LuD4130_assertion evidence source_evidence_literature NP908271.RA7mzPLroip5Iww5VnSwTyiQXYlzfVOu69jh3gKp7LuD4130_provenance.
- NP908271.RA7mzPLroip5Iww5VnSwTyiQXYlzfVOu69jh3gKp7LuD4130_assertion SIO_000772 21310059 NP908271.RA7mzPLroip5Iww5VnSwTyiQXYlzfVOu69jh3gKp7LuD4130_provenance.
- NP908271.RA7mzPLroip5Iww5VnSwTyiQXYlzfVOu69jh3gKp7LuD4130_assertion wasDerivedFrom befree-20140225 NP908271.RA7mzPLroip5Iww5VnSwTyiQXYlzfVOu69jh3gKp7LuD4130_provenance.
- NP908271.RA7mzPLroip5Iww5VnSwTyiQXYlzfVOu69jh3gKp7LuD4130_assertion wasGeneratedBy ECO_0000203 NP908271.RA7mzPLroip5Iww5VnSwTyiQXYlzfVOu69jh3gKp7LuD4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP908271.RA7mzPLroip5Iww5VnSwTyiQXYlzfVOu69jh3gKp7LuD4130_provenance.