Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP523701.RAb4w_vrA9g-fhFKVwR0Kl0nlFF4q12qqiC9Gj1uSMkYs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP523701.RAb4w_vrA9g-fhFKVwR0Kl0nlFF4q12qqiC9Gj1uSMkYs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523701.RAb4w_vrA9g-fhFKVwR0Kl0nlFF4q12qqiC9Gj1uSMkYs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523701.RAb4w_vrA9g-fhFKVwR0Kl0nlFF4q12qqiC9Gj1uSMkYs130_provenance.
- NP523701.RAb4w_vrA9g-fhFKVwR0Kl0nlFF4q12qqiC9Gj1uSMkYs130_assertion description "[Mutations in the MLC1 gene have been found as causative of MLC in 60-70 % of affected subjects, without genotype-phenotype correlation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523701.RAb4w_vrA9g-fhFKVwR0Kl0nlFF4q12qqiC9Gj1uSMkYs130_provenance.
- NP523701.RAb4w_vrA9g-fhFKVwR0Kl0nlFF4q12qqiC9Gj1uSMkYs130_assertion evidence source_evidence_literature NP523701.RAb4w_vrA9g-fhFKVwR0Kl0nlFF4q12qqiC9Gj1uSMkYs130_provenance.
- NP523701.RAb4w_vrA9g-fhFKVwR0Kl0nlFF4q12qqiC9Gj1uSMkYs130_assertion SIO_000772 21487377 NP523701.RAb4w_vrA9g-fhFKVwR0Kl0nlFF4q12qqiC9Gj1uSMkYs130_provenance.
- NP523701.RAb4w_vrA9g-fhFKVwR0Kl0nlFF4q12qqiC9Gj1uSMkYs130_assertion wasDerivedFrom befree-20140225 NP523701.RAb4w_vrA9g-fhFKVwR0Kl0nlFF4q12qqiC9Gj1uSMkYs130_provenance.
- NP523701.RAb4w_vrA9g-fhFKVwR0Kl0nlFF4q12qqiC9Gj1uSMkYs130_assertion wasGeneratedBy ECO_0000203 NP523701.RAb4w_vrA9g-fhFKVwR0Kl0nlFF4q12qqiC9Gj1uSMkYs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP523701.RAb4w_vrA9g-fhFKVwR0Kl0nlFF4q12qqiC9Gj1uSMkYs130_provenance.