Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP710426.RAbsanV16UvCaCPnztz3uwtnX77tT_p9vQ11gePCo4Ao4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP710426.RAbsanV16UvCaCPnztz3uwtnX77tT_p9vQ11gePCo4Ao4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710426.RAbsanV16UvCaCPnztz3uwtnX77tT_p9vQ11gePCo4Ao4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710426.RAbsanV16UvCaCPnztz3uwtnX77tT_p9vQ11gePCo4Ao4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP710426.RAbsanV16UvCaCPnztz3uwtnX77tT_p9vQ11gePCo4Ao4130_provenance.
- NP710426.RAbsanV16UvCaCPnztz3uwtnX77tT_p9vQ11gePCo4Ao4130_assertion wasGeneratedBy ECO_0000203 NP710426.RAbsanV16UvCaCPnztz3uwtnX77tT_p9vQ11gePCo4Ao4130_provenance.
- NP710426.RAbsanV16UvCaCPnztz3uwtnX77tT_p9vQ11gePCo4Ao4130_assertion wasDerivedFrom befree-20150227 NP710426.RAbsanV16UvCaCPnztz3uwtnX77tT_p9vQ11gePCo4Ao4130_provenance.
- NP710426.RAbsanV16UvCaCPnztz3uwtnX77tT_p9vQ11gePCo4Ao4130_assertion SIO_000772 19657220 NP710426.RAbsanV16UvCaCPnztz3uwtnX77tT_p9vQ11gePCo4Ao4130_provenance.
- NP710426.RAbsanV16UvCaCPnztz3uwtnX77tT_p9vQ11gePCo4Ao4130_assertion evidence source_evidence_literature NP710426.RAbsanV16UvCaCPnztz3uwtnX77tT_p9vQ11gePCo4Ao4130_provenance.
- NP710426.RAbsanV16UvCaCPnztz3uwtnX77tT_p9vQ11gePCo4Ao4130_assertion description "[The aim of this study was to determine for the first time the significance of PRSS1, SPINK1 mutations and genetic variants of AAT in a group of Spanish patients with CP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710426.RAbsanV16UvCaCPnztz3uwtnX77tT_p9vQ11gePCo4Ao4130_provenance.