Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP700546.RAAmKP1ZtQzdLitGphYH0-VITrWyjYhUvqwCkyVj45Sjs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP700546.RAAmKP1ZtQzdLitGphYH0-VITrWyjYhUvqwCkyVj45Sjs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP700546.RAAmKP1ZtQzdLitGphYH0-VITrWyjYhUvqwCkyVj45Sjs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP700546.RAAmKP1ZtQzdLitGphYH0-VITrWyjYhUvqwCkyVj45Sjs130_provenance.
- NP700546.RAAmKP1ZtQzdLitGphYH0-VITrWyjYhUvqwCkyVj45Sjs130_assertion description "[Polymorphisms in the genes encoding the 4 RET ligands, GDNF, NTN, ARTN, PSPN, and susceptibility to Hirschsprung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP700546.RAAmKP1ZtQzdLitGphYH0-VITrWyjYhUvqwCkyVj45Sjs130_provenance.
- NP700546.RAAmKP1ZtQzdLitGphYH0-VITrWyjYhUvqwCkyVj45Sjs130_assertion evidence source_evidence_literature NP700546.RAAmKP1ZtQzdLitGphYH0-VITrWyjYhUvqwCkyVj45Sjs130_provenance.
- NP700546.RAAmKP1ZtQzdLitGphYH0-VITrWyjYhUvqwCkyVj45Sjs130_assertion SIO_000772 18970938 NP700546.RAAmKP1ZtQzdLitGphYH0-VITrWyjYhUvqwCkyVj45Sjs130_provenance.
- NP700546.RAAmKP1ZtQzdLitGphYH0-VITrWyjYhUvqwCkyVj45Sjs130_assertion wasDerivedFrom befree-2016 NP700546.RAAmKP1ZtQzdLitGphYH0-VITrWyjYhUvqwCkyVj45Sjs130_provenance.
- NP700546.RAAmKP1ZtQzdLitGphYH0-VITrWyjYhUvqwCkyVj45Sjs130_assertion wasGeneratedBy ECO_0000203 NP700546.RAAmKP1ZtQzdLitGphYH0-VITrWyjYhUvqwCkyVj45Sjs130_provenance.
- befree-2016 importedOn "2016-02-19" NP700546.RAAmKP1ZtQzdLitGphYH0-VITrWyjYhUvqwCkyVj45Sjs130_provenance.