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- source_evidence_literature type ECO_0000212 NP644171.RAse5F4bdUfIOzan_4r0S7Lpv4QCd6o2sN9Av_qdl0Wng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP644171.RAse5F4bdUfIOzan_4r0S7Lpv4QCd6o2sN9Av_qdl0Wng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP644171.RAse5F4bdUfIOzan_4r0S7Lpv4QCd6o2sN9Av_qdl0Wng130_provenance.
- NP644171.RAse5F4bdUfIOzan_4r0S7Lpv4QCd6o2sN9Av_qdl0Wng130_assertion description "[We therefore determine in this study the relative frequency of mutations in PLCE1, WT1 or LAMB2 as the cause of IDMS in a worldwide cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP644171.RAse5F4bdUfIOzan_4r0S7Lpv4QCd6o2sN9Av_qdl0Wng130_provenance.
- NP644171.RAse5F4bdUfIOzan_4r0S7Lpv4QCd6o2sN9Av_qdl0Wng130_assertion evidence source_evidence_literature NP644171.RAse5F4bdUfIOzan_4r0S7Lpv4QCd6o2sN9Av_qdl0Wng130_provenance.
- NP644171.RAse5F4bdUfIOzan_4r0S7Lpv4QCd6o2sN9Av_qdl0Wng130_assertion SIO_000772 18065803 NP644171.RAse5F4bdUfIOzan_4r0S7Lpv4QCd6o2sN9Av_qdl0Wng130_provenance.
- NP644171.RAse5F4bdUfIOzan_4r0S7Lpv4QCd6o2sN9Av_qdl0Wng130_assertion wasDerivedFrom befree-2016 NP644171.RAse5F4bdUfIOzan_4r0S7Lpv4QCd6o2sN9Av_qdl0Wng130_provenance.
- NP644171.RAse5F4bdUfIOzan_4r0S7Lpv4QCd6o2sN9Av_qdl0Wng130_assertion wasGeneratedBy ECO_0000203 NP644171.RAse5F4bdUfIOzan_4r0S7Lpv4QCd6o2sN9Av_qdl0Wng130_provenance.
- befree-2016 importedOn "2016-02-19" NP644171.RAse5F4bdUfIOzan_4r0S7Lpv4QCd6o2sN9Av_qdl0Wng130_provenance.