Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP435990.RA2rW-y0-DDEtnPHNavS27fdPI8gW8UcGf_uv4_gLhCnk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP435990.RA2rW-y0-DDEtnPHNavS27fdPI8gW8UcGf_uv4_gLhCnk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP435990.RA2rW-y0-DDEtnPHNavS27fdPI8gW8UcGf_uv4_gLhCnk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP435990.RA2rW-y0-DDEtnPHNavS27fdPI8gW8UcGf_uv4_gLhCnk130_provenance.
- NP435990.RA2rW-y0-DDEtnPHNavS27fdPI8gW8UcGf_uv4_gLhCnk130_assertion description "[These results indicated that the polymorphism -9C>T and 368A>G in H2BFWT gene are associated with male infertility with idiopathic azoospermia or oligozoospermia, suggesting that H2BFWT gene might be contribute to susceptibility to spermatogenesis impairment in Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435990.RA2rW-y0-DDEtnPHNavS27fdPI8gW8UcGf_uv4_gLhCnk130_provenance.
- NP435990.RA2rW-y0-DDEtnPHNavS27fdPI8gW8UcGf_uv4_gLhCnk130_assertion evidence source_evidence_literature NP435990.RA2rW-y0-DDEtnPHNavS27fdPI8gW8UcGf_uv4_gLhCnk130_provenance.
- NP435990.RA2rW-y0-DDEtnPHNavS27fdPI8gW8UcGf_uv4_gLhCnk130_assertion SIO_000772 22509975 NP435990.RA2rW-y0-DDEtnPHNavS27fdPI8gW8UcGf_uv4_gLhCnk130_provenance.
- NP435990.RA2rW-y0-DDEtnPHNavS27fdPI8gW8UcGf_uv4_gLhCnk130_assertion wasDerivedFrom befree-20140225 NP435990.RA2rW-y0-DDEtnPHNavS27fdPI8gW8UcGf_uv4_gLhCnk130_provenance.
- NP435990.RA2rW-y0-DDEtnPHNavS27fdPI8gW8UcGf_uv4_gLhCnk130_assertion wasGeneratedBy ECO_0000203 NP435990.RA2rW-y0-DDEtnPHNavS27fdPI8gW8UcGf_uv4_gLhCnk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP435990.RA2rW-y0-DDEtnPHNavS27fdPI8gW8UcGf_uv4_gLhCnk130_provenance.