Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP523701.RAb4w_vrA9g-fhFKVwR0Kl0nlFF4q12qqiC9Gj1uSMkYs130_assertion> ?p ?o ?g. }
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- NP523701.RAb4w_vrA9g-fhFKVwR0Kl0nlFF4q12qqiC9Gj1uSMkYs130_assertion type Assertion NP523701.RAb4w_vrA9g-fhFKVwR0Kl0nlFF4q12qqiC9Gj1uSMkYs130_head.
- 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.