Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP648535.RAug0_QLQtkGFGoHTeglogG73o5uGHVP0mJrt3ee7O_MY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP648535.RAug0_QLQtkGFGoHTeglogG73o5uGHVP0mJrt3ee7O_MY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP648535.RAug0_QLQtkGFGoHTeglogG73o5uGHVP0mJrt3ee7O_MY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP648535.RAug0_QLQtkGFGoHTeglogG73o5uGHVP0mJrt3ee7O_MY130_provenance.
- NP648535.RAug0_QLQtkGFGoHTeglogG73o5uGHVP0mJrt3ee7O_MY130_assertion description "[XRCC4 promoter -1394( *)T-related genotype/alleles are associated with higher susceptibility of leiomyoma, whereas XRCC4 codon 247, XRCC4 intron 3, XPD codon 312, XPD codon 751, and XPD promoter -114 polymorphisms are not correlated with its development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648535.RAug0_QLQtkGFGoHTeglogG73o5uGHVP0mJrt3ee7O_MY130_provenance.
- NP648535.RAug0_QLQtkGFGoHTeglogG73o5uGHVP0mJrt3ee7O_MY130_assertion evidence source_evidence_literature NP648535.RAug0_QLQtkGFGoHTeglogG73o5uGHVP0mJrt3ee7O_MY130_provenance.
- NP648535.RAug0_QLQtkGFGoHTeglogG73o5uGHVP0mJrt3ee7O_MY130_assertion SIO_000772 18177646 NP648535.RAug0_QLQtkGFGoHTeglogG73o5uGHVP0mJrt3ee7O_MY130_provenance.
- NP648535.RAug0_QLQtkGFGoHTeglogG73o5uGHVP0mJrt3ee7O_MY130_assertion wasDerivedFrom befree-2016 NP648535.RAug0_QLQtkGFGoHTeglogG73o5uGHVP0mJrt3ee7O_MY130_provenance.
- NP648535.RAug0_QLQtkGFGoHTeglogG73o5uGHVP0mJrt3ee7O_MY130_assertion wasGeneratedBy ECO_0000203 NP648535.RAug0_QLQtkGFGoHTeglogG73o5uGHVP0mJrt3ee7O_MY130_provenance.
- befree-2016 importedOn "2016-02-19" NP648535.RAug0_QLQtkGFGoHTeglogG73o5uGHVP0mJrt3ee7O_MY130_provenance.