Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP156982.RAIAeEnR3w34C3cgZRrsrLSSHFukeVmU9ZlVnJ_hu-8Ow130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP156982.RAIAeEnR3w34C3cgZRrsrLSSHFukeVmU9ZlVnJ_hu-8Ow130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP156982.RAIAeEnR3w34C3cgZRrsrLSSHFukeVmU9ZlVnJ_hu-8Ow130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP156982.RAIAeEnR3w34C3cgZRrsrLSSHFukeVmU9ZlVnJ_hu-8Ow130_provenance.
- NP156982.RAIAeEnR3w34C3cgZRrsrLSSHFukeVmU9ZlVnJ_hu-8Ow130_assertion description "[Since SPINK1 mutations in Europeans and North Americans are associated with idiopathic chronic pancreatitis that is phenotypically different from FCPD, we further conclude that mutated SPINK1 markedly increases the risk of developing a variety of pancreatic diseases possibly through a chronic elevation of active trypsin within the pancreas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP156982.RAIAeEnR3w34C3cgZRrsrLSSHFukeVmU9ZlVnJ_hu-8Ow130_provenance.
- NP156982.RAIAeEnR3w34C3cgZRrsrLSSHFukeVmU9ZlVnJ_hu-8Ow130_assertion evidence source_evidence_literature NP156982.RAIAeEnR3w34C3cgZRrsrLSSHFukeVmU9ZlVnJ_hu-8Ow130_provenance.
- NP156982.RAIAeEnR3w34C3cgZRrsrLSSHFukeVmU9ZlVnJ_hu-8Ow130_assertion SIO_000772 12120202 NP156982.RAIAeEnR3w34C3cgZRrsrLSSHFukeVmU9ZlVnJ_hu-8Ow130_provenance.
- NP156982.RAIAeEnR3w34C3cgZRrsrLSSHFukeVmU9ZlVnJ_hu-8Ow130_assertion wasDerivedFrom befree-20140225 NP156982.RAIAeEnR3w34C3cgZRrsrLSSHFukeVmU9ZlVnJ_hu-8Ow130_provenance.
- NP156982.RAIAeEnR3w34C3cgZRrsrLSSHFukeVmU9ZlVnJ_hu-8Ow130_assertion wasGeneratedBy ECO_0000203 NP156982.RAIAeEnR3w34C3cgZRrsrLSSHFukeVmU9ZlVnJ_hu-8Ow130_provenance.
- befree-20140225 importedOn "2014-02-25" NP156982.RAIAeEnR3w34C3cgZRrsrLSSHFukeVmU9ZlVnJ_hu-8Ow130_provenance.