Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP68751.RA9aHleBm_FGaB4aCdl0Ov0_fkB7G8S2LhnIb_SVImins130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP68751.RA9aHleBm_FGaB4aCdl0Ov0_fkB7G8S2LhnIb_SVImins130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP68751.RA9aHleBm_FGaB4aCdl0Ov0_fkB7G8S2LhnIb_SVImins130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP68751.RA9aHleBm_FGaB4aCdl0Ov0_fkB7G8S2LhnIb_SVImins130_provenance.
- NP68751.RA9aHleBm_FGaB4aCdl0Ov0_fkB7G8S2LhnIb_SVImins130_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." NP68751.RA9aHleBm_FGaB4aCdl0Ov0_fkB7G8S2LhnIb_SVImins130_provenance.
- NP68751.RA9aHleBm_FGaB4aCdl0Ov0_fkB7G8S2LhnIb_SVImins130_assertion evidence source_evidence_literature NP68751.RA9aHleBm_FGaB4aCdl0Ov0_fkB7G8S2LhnIb_SVImins130_provenance.
- NP68751.RA9aHleBm_FGaB4aCdl0Ov0_fkB7G8S2LhnIb_SVImins130_assertion SIO_000772 18970938 NP68751.RA9aHleBm_FGaB4aCdl0Ov0_fkB7G8S2LhnIb_SVImins130_provenance.
- NP68751.RA9aHleBm_FGaB4aCdl0Ov0_fkB7G8S2LhnIb_SVImins130_assertion wasDerivedFrom gad-20130706 NP68751.RA9aHleBm_FGaB4aCdl0Ov0_fkB7G8S2LhnIb_SVImins130_provenance.
- NP68751.RA9aHleBm_FGaB4aCdl0Ov0_fkB7G8S2LhnIb_SVImins130_assertion wasGeneratedBy ECO_0000203 NP68751.RA9aHleBm_FGaB4aCdl0Ov0_fkB7G8S2LhnIb_SVImins130_provenance.
- gad-20130706 importedOn "2013-07-06" NP68751.RA9aHleBm_FGaB4aCdl0Ov0_fkB7G8S2LhnIb_SVImins130_provenance.