Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP343977.RATbE5-D2ASllb1Bqv3feL9f1pOvi8sbkwjh9SXqVZA68130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP343977.RATbE5-D2ASllb1Bqv3feL9f1pOvi8sbkwjh9SXqVZA68130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343977.RATbE5-D2ASllb1Bqv3feL9f1pOvi8sbkwjh9SXqVZA68130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343977.RATbE5-D2ASllb1Bqv3feL9f1pOvi8sbkwjh9SXqVZA68130_provenance.
- befree-2016 importedOn "2016-02-19" NP343977.RATbE5-D2ASllb1Bqv3feL9f1pOvi8sbkwjh9SXqVZA68130_provenance.
- NP343977.RATbE5-D2ASllb1Bqv3feL9f1pOvi8sbkwjh9SXqVZA68130_assertion wasGeneratedBy ECO_0000203 NP343977.RATbE5-D2ASllb1Bqv3feL9f1pOvi8sbkwjh9SXqVZA68130_provenance.
- NP343977.RATbE5-D2ASllb1Bqv3feL9f1pOvi8sbkwjh9SXqVZA68130_assertion wasDerivedFrom befree-2016 NP343977.RATbE5-D2ASllb1Bqv3feL9f1pOvi8sbkwjh9SXqVZA68130_provenance.
- NP343977.RATbE5-D2ASllb1Bqv3feL9f1pOvi8sbkwjh9SXqVZA68130_assertion SIO_000772 11826022 NP343977.RATbE5-D2ASllb1Bqv3feL9f1pOvi8sbkwjh9SXqVZA68130_provenance.
- NP343977.RATbE5-D2ASllb1Bqv3feL9f1pOvi8sbkwjh9SXqVZA68130_assertion evidence source_evidence_literature NP343977.RATbE5-D2ASllb1Bqv3feL9f1pOvi8sbkwjh9SXqVZA68130_provenance.
- NP343977.RATbE5-D2ASllb1Bqv3feL9f1pOvi8sbkwjh9SXqVZA68130_assertion description "[These results indicate that CSGE is highly sensitive for the detection of mutations in FBN1, and that molecular diagnostics is a useful means of confirming clinical diagnoses of MFS and related disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343977.RATbE5-D2ASllb1Bqv3feL9f1pOvi8sbkwjh9SXqVZA68130_provenance.