Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP547221.RAytHRTb2JfAMxPp_EsuxlobCC-MEVBhnUKDFzEAOOFD0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP547221.RAytHRTb2JfAMxPp_EsuxlobCC-MEVBhnUKDFzEAOOFD0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP547221.RAytHRTb2JfAMxPp_EsuxlobCC-MEVBhnUKDFzEAOOFD0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP547221.RAytHRTb2JfAMxPp_EsuxlobCC-MEVBhnUKDFzEAOOFD0130_provenance.
- NP547221.RAytHRTb2JfAMxPp_EsuxlobCC-MEVBhnUKDFzEAOOFD0130_assertion description "[Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547221.RAytHRTb2JfAMxPp_EsuxlobCC-MEVBhnUKDFzEAOOFD0130_provenance.
- NP547221.RAytHRTb2JfAMxPp_EsuxlobCC-MEVBhnUKDFzEAOOFD0130_assertion evidence source_evidence_literature NP547221.RAytHRTb2JfAMxPp_EsuxlobCC-MEVBhnUKDFzEAOOFD0130_provenance.
- NP547221.RAytHRTb2JfAMxPp_EsuxlobCC-MEVBhnUKDFzEAOOFD0130_assertion SIO_000772 16645022 NP547221.RAytHRTb2JfAMxPp_EsuxlobCC-MEVBhnUKDFzEAOOFD0130_provenance.
- NP547221.RAytHRTb2JfAMxPp_EsuxlobCC-MEVBhnUKDFzEAOOFD0130_assertion wasDerivedFrom befree-2016 NP547221.RAytHRTb2JfAMxPp_EsuxlobCC-MEVBhnUKDFzEAOOFD0130_provenance.
- NP547221.RAytHRTb2JfAMxPp_EsuxlobCC-MEVBhnUKDFzEAOOFD0130_assertion wasGeneratedBy ECO_0000203 NP547221.RAytHRTb2JfAMxPp_EsuxlobCC-MEVBhnUKDFzEAOOFD0130_provenance.
- befree-2016 importedOn "2016-02-19" NP547221.RAytHRTb2JfAMxPp_EsuxlobCC-MEVBhnUKDFzEAOOFD0130_provenance.