Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP523080.RARWSSl7UBKlZlkw8yQ7bmvD_fRlOWg261e6WDXT6iWzs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP523080.RARWSSl7UBKlZlkw8yQ7bmvD_fRlOWg261e6WDXT6iWzs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523080.RARWSSl7UBKlZlkw8yQ7bmvD_fRlOWg261e6WDXT6iWzs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523080.RARWSSl7UBKlZlkw8yQ7bmvD_fRlOWg261e6WDXT6iWzs130_provenance.
- NP523080.RARWSSl7UBKlZlkw8yQ7bmvD_fRlOWg261e6WDXT6iWzs130_assertion description "[Results of the present study indicate that SNP IVS6+55G-->T and c.852C-->T of GRTH gene may be associated with male infertility with azoospermia or severe oligozoospermia, suggesting that variations in GRTH gene may contribute to susceptibility to spermatogenic impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523080.RARWSSl7UBKlZlkw8yQ7bmvD_fRlOWg261e6WDXT6iWzs130_provenance.
- NP523080.RARWSSl7UBKlZlkw8yQ7bmvD_fRlOWg261e6WDXT6iWzs130_assertion evidence source_evidence_literature NP523080.RARWSSl7UBKlZlkw8yQ7bmvD_fRlOWg261e6WDXT6iWzs130_provenance.
- NP523080.RARWSSl7UBKlZlkw8yQ7bmvD_fRlOWg261e6WDXT6iWzs130_assertion SIO_000772 16293649 NP523080.RARWSSl7UBKlZlkw8yQ7bmvD_fRlOWg261e6WDXT6iWzs130_provenance.
- NP523080.RARWSSl7UBKlZlkw8yQ7bmvD_fRlOWg261e6WDXT6iWzs130_assertion wasDerivedFrom befree-2016 NP523080.RARWSSl7UBKlZlkw8yQ7bmvD_fRlOWg261e6WDXT6iWzs130_provenance.
- NP523080.RARWSSl7UBKlZlkw8yQ7bmvD_fRlOWg261e6WDXT6iWzs130_assertion wasGeneratedBy ECO_0000203 NP523080.RARWSSl7UBKlZlkw8yQ7bmvD_fRlOWg261e6WDXT6iWzs130_provenance.
- befree-2016 importedOn "2016-02-19" NP523080.RARWSSl7UBKlZlkw8yQ7bmvD_fRlOWg261e6WDXT6iWzs130_provenance.