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- source_evidence_literature type ECO_0000212 NP972181.RA9gikMAdFKE6_afL98R528eQhRxmLgPfssosrKnKqChk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP972181.RA9gikMAdFKE6_afL98R528eQhRxmLgPfssosrKnKqChk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP972181.RA9gikMAdFKE6_afL98R528eQhRxmLgPfssosrKnKqChk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP972181.RA9gikMAdFKE6_afL98R528eQhRxmLgPfssosrKnKqChk130_provenance.
- NP972181.RA9gikMAdFKE6_afL98R528eQhRxmLgPfssosrKnKqChk130_assertion wasGeneratedBy ECO_0000203 NP972181.RA9gikMAdFKE6_afL98R528eQhRxmLgPfssosrKnKqChk130_provenance.
- NP972181.RA9gikMAdFKE6_afL98R528eQhRxmLgPfssosrKnKqChk130_assertion wasDerivedFrom befree-20150227 NP972181.RA9gikMAdFKE6_afL98R528eQhRxmLgPfssosrKnKqChk130_provenance.
- NP972181.RA9gikMAdFKE6_afL98R528eQhRxmLgPfssosrKnKqChk130_assertion SIO_000772 19657220 NP972181.RA9gikMAdFKE6_afL98R528eQhRxmLgPfssosrKnKqChk130_provenance.
- NP972181.RA9gikMAdFKE6_afL98R528eQhRxmLgPfssosrKnKqChk130_assertion evidence source_evidence_literature NP972181.RA9gikMAdFKE6_afL98R528eQhRxmLgPfssosrKnKqChk130_provenance.
- NP972181.RA9gikMAdFKE6_afL98R528eQhRxmLgPfssosrKnKqChk130_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." NP972181.RA9gikMAdFKE6_afL98R528eQhRxmLgPfssosrKnKqChk130_provenance.