Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP330996.RAdE3NlPH8DeXdcAXhMPv3oCOsK52Eg6jWhPJ7dRpVh_c130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP330996.RAdE3NlPH8DeXdcAXhMPv3oCOsK52Eg6jWhPJ7dRpVh_c130_assertion type Assertion NP330996.RAdE3NlPH8DeXdcAXhMPv3oCOsK52Eg6jWhPJ7dRpVh_c130_head.
- NP330996.RAdE3NlPH8DeXdcAXhMPv3oCOsK52Eg6jWhPJ7dRpVh_c130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330996.RAdE3NlPH8DeXdcAXhMPv3oCOsK52Eg6jWhPJ7dRpVh_c130_provenance.
- NP330996.RAdE3NlPH8DeXdcAXhMPv3oCOsK52Eg6jWhPJ7dRpVh_c130_assertion evidence source_evidence_literature NP330996.RAdE3NlPH8DeXdcAXhMPv3oCOsK52Eg6jWhPJ7dRpVh_c130_provenance.
- NP330996.RAdE3NlPH8DeXdcAXhMPv3oCOsK52Eg6jWhPJ7dRpVh_c130_assertion SIO_000772 10496225 NP330996.RAdE3NlPH8DeXdcAXhMPv3oCOsK52Eg6jWhPJ7dRpVh_c130_provenance.
- NP330996.RAdE3NlPH8DeXdcAXhMPv3oCOsK52Eg6jWhPJ7dRpVh_c130_assertion wasDerivedFrom befree-20140225 NP330996.RAdE3NlPH8DeXdcAXhMPv3oCOsK52Eg6jWhPJ7dRpVh_c130_provenance.
- NP330996.RAdE3NlPH8DeXdcAXhMPv3oCOsK52Eg6jWhPJ7dRpVh_c130_assertion wasGeneratedBy ECO_0000203 NP330996.RAdE3NlPH8DeXdcAXhMPv3oCOsK52Eg6jWhPJ7dRpVh_c130_provenance.