Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_assertion> ?p ?o ?g. }
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- NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_assertion type Assertion NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_head.
- NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_assertion description "[Abnormalities of peripheral myelin protein 22 (PMP-22) account for dominantly inherited HMSN type I in approximately 90% of families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_provenance.
- NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_assertion evidence source_evidence_literature NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_provenance.
- NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_assertion SIO_000772 7541290 NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_provenance.
- NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_assertion wasDerivedFrom befree-20140225 NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_provenance.
- NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_assertion wasGeneratedBy ECO_0000203 NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_provenance.