Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP596387.RAqVx1JyynMfCDF0_E2Y2s3OZsPoMv57AFjQX3nng1ew4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP596387.RAqVx1JyynMfCDF0_E2Y2s3OZsPoMv57AFjQX3nng1ew4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP596387.RAqVx1JyynMfCDF0_E2Y2s3OZsPoMv57AFjQX3nng1ew4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP596387.RAqVx1JyynMfCDF0_E2Y2s3OZsPoMv57AFjQX3nng1ew4130_provenance.
- NP596387.RAqVx1JyynMfCDF0_E2Y2s3OZsPoMv57AFjQX3nng1ew4130_assertion description "[Based on a structured questionnaire and medical records, the authors found that 12 of 25 mothers with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with the R133C NOTCH3 mutation had had neurologic symptoms in 17 of their 43 pregnancies, most commonly hemiparesthesia (76%), hemiparesis (36%), aphasia (65%), and visual disorders (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP596387.RAqVx1JyynMfCDF0_E2Y2s3OZsPoMv57AFjQX3nng1ew4130_provenance.
- NP596387.RAqVx1JyynMfCDF0_E2Y2s3OZsPoMv57AFjQX3nng1ew4130_assertion evidence source_evidence_literature NP596387.RAqVx1JyynMfCDF0_E2Y2s3OZsPoMv57AFjQX3nng1ew4130_provenance.
- NP596387.RAqVx1JyynMfCDF0_E2Y2s3OZsPoMv57AFjQX3nng1ew4130_assertion SIO_000772 15851739 NP596387.RAqVx1JyynMfCDF0_E2Y2s3OZsPoMv57AFjQX3nng1ew4130_provenance.
- NP596387.RAqVx1JyynMfCDF0_E2Y2s3OZsPoMv57AFjQX3nng1ew4130_assertion wasDerivedFrom befree-20150227 NP596387.RAqVx1JyynMfCDF0_E2Y2s3OZsPoMv57AFjQX3nng1ew4130_provenance.
- NP596387.RAqVx1JyynMfCDF0_E2Y2s3OZsPoMv57AFjQX3nng1ew4130_assertion wasGeneratedBy ECO_0000203 NP596387.RAqVx1JyynMfCDF0_E2Y2s3OZsPoMv57AFjQX3nng1ew4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP596387.RAqVx1JyynMfCDF0_E2Y2s3OZsPoMv57AFjQX3nng1ew4130_provenance.