Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP328717.RAqblUcxJ4BlbD82cOIPFdSs7W1FKrenPYNMxOmEo5iic130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP328717.RAqblUcxJ4BlbD82cOIPFdSs7W1FKrenPYNMxOmEo5iic130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP328717.RAqblUcxJ4BlbD82cOIPFdSs7W1FKrenPYNMxOmEo5iic130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP328717.RAqblUcxJ4BlbD82cOIPFdSs7W1FKrenPYNMxOmEo5iic130_provenance.
- NP328717.RAqblUcxJ4BlbD82cOIPFdSs7W1FKrenPYNMxOmEo5iic130_assertion description "[To analyze the distribution of the single nucleotide polymorphism (SNP) C677T in the methylenetetrahydrofolate reductase (MTHFR) gene in 355 infertile Chinese patients with idiopathic azoospermia or severe oligozoospermia and 252 fertile Chinese men as controls to explore the possible association of the SNP and male infertility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328717.RAqblUcxJ4BlbD82cOIPFdSs7W1FKrenPYNMxOmEo5iic130_provenance.
- NP328717.RAqblUcxJ4BlbD82cOIPFdSs7W1FKrenPYNMxOmEo5iic130_assertion evidence source_evidence_literature NP328717.RAqblUcxJ4BlbD82cOIPFdSs7W1FKrenPYNMxOmEo5iic130_provenance.
- NP328717.RAqblUcxJ4BlbD82cOIPFdSs7W1FKrenPYNMxOmEo5iic130_assertion SIO_000772 16888682 NP328717.RAqblUcxJ4BlbD82cOIPFdSs7W1FKrenPYNMxOmEo5iic130_provenance.
- NP328717.RAqblUcxJ4BlbD82cOIPFdSs7W1FKrenPYNMxOmEo5iic130_assertion wasDerivedFrom befree-20140225 NP328717.RAqblUcxJ4BlbD82cOIPFdSs7W1FKrenPYNMxOmEo5iic130_provenance.
- NP328717.RAqblUcxJ4BlbD82cOIPFdSs7W1FKrenPYNMxOmEo5iic130_assertion wasGeneratedBy ECO_0000203 NP328717.RAqblUcxJ4BlbD82cOIPFdSs7W1FKrenPYNMxOmEo5iic130_provenance.
- befree-20140225 importedOn "2014-02-25" NP328717.RAqblUcxJ4BlbD82cOIPFdSs7W1FKrenPYNMxOmEo5iic130_provenance.