Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP693762.RAcz-7LcxrSMNrLDbwvIfvlW_rdWT4RtnVDGxdAZ3ndWg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP693762.RAcz-7LcxrSMNrLDbwvIfvlW_rdWT4RtnVDGxdAZ3ndWg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP693762.RAcz-7LcxrSMNrLDbwvIfvlW_rdWT4RtnVDGxdAZ3ndWg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP693762.RAcz-7LcxrSMNrLDbwvIfvlW_rdWT4RtnVDGxdAZ3ndWg130_provenance.
- NP693762.RAcz-7LcxrSMNrLDbwvIfvlW_rdWT4RtnVDGxdAZ3ndWg130_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." NP693762.RAcz-7LcxrSMNrLDbwvIfvlW_rdWT4RtnVDGxdAZ3ndWg130_provenance.
- NP693762.RAcz-7LcxrSMNrLDbwvIfvlW_rdWT4RtnVDGxdAZ3ndWg130_assertion evidence source_evidence_literature NP693762.RAcz-7LcxrSMNrLDbwvIfvlW_rdWT4RtnVDGxdAZ3ndWg130_provenance.
- NP693762.RAcz-7LcxrSMNrLDbwvIfvlW_rdWT4RtnVDGxdAZ3ndWg130_assertion SIO_000772 18970938 NP693762.RAcz-7LcxrSMNrLDbwvIfvlW_rdWT4RtnVDGxdAZ3ndWg130_provenance.
- NP693762.RAcz-7LcxrSMNrLDbwvIfvlW_rdWT4RtnVDGxdAZ3ndWg130_assertion wasDerivedFrom befree-20140225 NP693762.RAcz-7LcxrSMNrLDbwvIfvlW_rdWT4RtnVDGxdAZ3ndWg130_provenance.
- NP693762.RAcz-7LcxrSMNrLDbwvIfvlW_rdWT4RtnVDGxdAZ3ndWg130_assertion wasGeneratedBy ECO_0000203 NP693762.RAcz-7LcxrSMNrLDbwvIfvlW_rdWT4RtnVDGxdAZ3ndWg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP693762.RAcz-7LcxrSMNrLDbwvIfvlW_rdWT4RtnVDGxdAZ3ndWg130_provenance.