Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP430282.RAKOnsrz1R1mO2C1xUF9Wrp_nEyvm4R4MmsUB_4oeoZf8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP430282.RAKOnsrz1R1mO2C1xUF9Wrp_nEyvm4R4MmsUB_4oeoZf8130_assertion type Assertion NP430282.RAKOnsrz1R1mO2C1xUF9Wrp_nEyvm4R4MmsUB_4oeoZf8130_head.
- NP430282.RAKOnsrz1R1mO2C1xUF9Wrp_nEyvm4R4MmsUB_4oeoZf8130_assertion description "[In the majority of cases HNPP is caused by deletion of the peripheral myelin protein 22 gene (PMP22) on chromosome 17p11.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430282.RAKOnsrz1R1mO2C1xUF9Wrp_nEyvm4R4MmsUB_4oeoZf8130_provenance.
- NP430282.RAKOnsrz1R1mO2C1xUF9Wrp_nEyvm4R4MmsUB_4oeoZf8130_assertion evidence source_evidence_literature NP430282.RAKOnsrz1R1mO2C1xUF9Wrp_nEyvm4R4MmsUB_4oeoZf8130_provenance.
- NP430282.RAKOnsrz1R1mO2C1xUF9Wrp_nEyvm4R4MmsUB_4oeoZf8130_assertion SIO_000772 17183456 NP430282.RAKOnsrz1R1mO2C1xUF9Wrp_nEyvm4R4MmsUB_4oeoZf8130_provenance.
- NP430282.RAKOnsrz1R1mO2C1xUF9Wrp_nEyvm4R4MmsUB_4oeoZf8130_assertion wasDerivedFrom befree-20140225 NP430282.RAKOnsrz1R1mO2C1xUF9Wrp_nEyvm4R4MmsUB_4oeoZf8130_provenance.
- NP430282.RAKOnsrz1R1mO2C1xUF9Wrp_nEyvm4R4MmsUB_4oeoZf8130_assertion wasGeneratedBy ECO_0000203 NP430282.RAKOnsrz1R1mO2C1xUF9Wrp_nEyvm4R4MmsUB_4oeoZf8130_provenance.