Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP129961.RAtgUTp3LqVJuIHnpEGq5izNwuqo18tqKk6VuYseq0AAo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP129961.RAtgUTp3LqVJuIHnpEGq5izNwuqo18tqKk6VuYseq0AAo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP129961.RAtgUTp3LqVJuIHnpEGq5izNwuqo18tqKk6VuYseq0AAo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP129961.RAtgUTp3LqVJuIHnpEGq5izNwuqo18tqKk6VuYseq0AAo130_provenance.
- NP129961.RAtgUTp3LqVJuIHnpEGq5izNwuqo18tqKk6VuYseq0AAo130_assertion description "[Single nucleotide polymorphism C677T in the methylenetetrahydrofolate reductase gene might be a genetic risk factor for infertility for Chinese men with azoospermia or severe oligozoospermia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP129961.RAtgUTp3LqVJuIHnpEGq5izNwuqo18tqKk6VuYseq0AAo130_provenance.
- NP129961.RAtgUTp3LqVJuIHnpEGq5izNwuqo18tqKk6VuYseq0AAo130_assertion evidence source_evidence_literature NP129961.RAtgUTp3LqVJuIHnpEGq5izNwuqo18tqKk6VuYseq0AAo130_provenance.
- NP129961.RAtgUTp3LqVJuIHnpEGq5izNwuqo18tqKk6VuYseq0AAo130_assertion SIO_000772 16888682 NP129961.RAtgUTp3LqVJuIHnpEGq5izNwuqo18tqKk6VuYseq0AAo130_provenance.
- NP129961.RAtgUTp3LqVJuIHnpEGq5izNwuqo18tqKk6VuYseq0AAo130_assertion wasDerivedFrom gad-20150221 NP129961.RAtgUTp3LqVJuIHnpEGq5izNwuqo18tqKk6VuYseq0AAo130_provenance.
- NP129961.RAtgUTp3LqVJuIHnpEGq5izNwuqo18tqKk6VuYseq0AAo130_assertion wasGeneratedBy ECO_0000203 NP129961.RAtgUTp3LqVJuIHnpEGq5izNwuqo18tqKk6VuYseq0AAo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP129961.RAtgUTp3LqVJuIHnpEGq5izNwuqo18tqKk6VuYseq0AAo130_provenance.