Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1111032.RARq3HnvrJCB3KlpQ7Slw4UOIQcmC0Yk7jWhgSxSFNEus130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1111032.RARq3HnvrJCB3KlpQ7Slw4UOIQcmC0Yk7jWhgSxSFNEus130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1111032.RARq3HnvrJCB3KlpQ7Slw4UOIQcmC0Yk7jWhgSxSFNEus130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1111032.RARq3HnvrJCB3KlpQ7Slw4UOIQcmC0Yk7jWhgSxSFNEus130_provenance.
- NP1111032.RARq3HnvrJCB3KlpQ7Slw4UOIQcmC0Yk7jWhgSxSFNEus130_assertion description "[In our previous study, we have identified a homozygous TMEM67 mutation in a Chinese family exhibiting clinical characteristics of MKS3, which provided a ground for further PGD procedure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1111032.RARq3HnvrJCB3KlpQ7Slw4UOIQcmC0Yk7jWhgSxSFNEus130_provenance.
- NP1111032.RARq3HnvrJCB3KlpQ7Slw4UOIQcmC0Yk7jWhgSxSFNEus130_assertion evidence source_evidence_literature NP1111032.RARq3HnvrJCB3KlpQ7Slw4UOIQcmC0Yk7jWhgSxSFNEus130_provenance.
- NP1111032.RARq3HnvrJCB3KlpQ7Slw4UOIQcmC0Yk7jWhgSxSFNEus130_assertion SIO_000772 24039893 NP1111032.RARq3HnvrJCB3KlpQ7Slw4UOIQcmC0Yk7jWhgSxSFNEus130_provenance.
- NP1111032.RARq3HnvrJCB3KlpQ7Slw4UOIQcmC0Yk7jWhgSxSFNEus130_assertion wasDerivedFrom befree-2016 NP1111032.RARq3HnvrJCB3KlpQ7Slw4UOIQcmC0Yk7jWhgSxSFNEus130_provenance.
- NP1111032.RARq3HnvrJCB3KlpQ7Slw4UOIQcmC0Yk7jWhgSxSFNEus130_assertion wasGeneratedBy ECO_0000203 NP1111032.RARq3HnvrJCB3KlpQ7Slw4UOIQcmC0Yk7jWhgSxSFNEus130_provenance.
- befree-2016 importedOn "2016-02-19" NP1111032.RARq3HnvrJCB3KlpQ7Slw4UOIQcmC0Yk7jWhgSxSFNEus130_provenance.