Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_provenance.