Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP979451.RAf1VMW2jN73w__clV--ETrd4Hcq2SbP0BSoQfHFzmuzc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP979451.RAf1VMW2jN73w__clV--ETrd4Hcq2SbP0BSoQfHFzmuzc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP979451.RAf1VMW2jN73w__clV--ETrd4Hcq2SbP0BSoQfHFzmuzc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP979451.RAf1VMW2jN73w__clV--ETrd4Hcq2SbP0BSoQfHFzmuzc130_provenance.
- NP979451.RAf1VMW2jN73w__clV--ETrd4Hcq2SbP0BSoQfHFzmuzc130_assertion description "[Similarly, patients with a BHD germline mutation and family history of spontaneous pneumothorax had a significantly increased greater probability of having spontaneous pneumothorax than BHDS patients without a family history of spontaneous pneumothorax (p = 0.011).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP979451.RAf1VMW2jN73w__clV--ETrd4Hcq2SbP0BSoQfHFzmuzc130_provenance.
- NP979451.RAf1VMW2jN73w__clV--ETrd4Hcq2SbP0BSoQfHFzmuzc130_assertion evidence source_evidence_literature NP979451.RAf1VMW2jN73w__clV--ETrd4Hcq2SbP0BSoQfHFzmuzc130_provenance.
- NP979451.RAf1VMW2jN73w__clV--ETrd4Hcq2SbP0BSoQfHFzmuzc130_assertion SIO_000772 18234728 NP979451.RAf1VMW2jN73w__clV--ETrd4Hcq2SbP0BSoQfHFzmuzc130_provenance.
- NP979451.RAf1VMW2jN73w__clV--ETrd4Hcq2SbP0BSoQfHFzmuzc130_assertion wasDerivedFrom befree-20150227 NP979451.RAf1VMW2jN73w__clV--ETrd4Hcq2SbP0BSoQfHFzmuzc130_provenance.
- NP979451.RAf1VMW2jN73w__clV--ETrd4Hcq2SbP0BSoQfHFzmuzc130_assertion wasGeneratedBy ECO_0000203 NP979451.RAf1VMW2jN73w__clV--ETrd4Hcq2SbP0BSoQfHFzmuzc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP979451.RAf1VMW2jN73w__clV--ETrd4Hcq2SbP0BSoQfHFzmuzc130_provenance.