Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP164070.RARKtHbvtU6LZguEHMeYOwrzDSA8kjpLtmDLEWovFPIu0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP164070.RARKtHbvtU6LZguEHMeYOwrzDSA8kjpLtmDLEWovFPIu0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP164070.RARKtHbvtU6LZguEHMeYOwrzDSA8kjpLtmDLEWovFPIu0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP164070.RARKtHbvtU6LZguEHMeYOwrzDSA8kjpLtmDLEWovFPIu0130_provenance.
- NP164070.RARKtHbvtU6LZguEHMeYOwrzDSA8kjpLtmDLEWovFPIu0130_assertion description "[CDPX2 patients display skin defects including linear or whorled atrophic and pigmentary lesions, striated hyperkeratosis, coarse lusterless hair and alopecia, cataracts and skeletal abnormalities including short stature, rhizomelic shortening of the limbs, epiphyseal stippling and craniofacial defects (MIM 302960).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164070.RARKtHbvtU6LZguEHMeYOwrzDSA8kjpLtmDLEWovFPIu0130_provenance.
- NP164070.RARKtHbvtU6LZguEHMeYOwrzDSA8kjpLtmDLEWovFPIu0130_assertion evidence source_evidence_literature NP164070.RARKtHbvtU6LZguEHMeYOwrzDSA8kjpLtmDLEWovFPIu0130_provenance.
- NP164070.RARKtHbvtU6LZguEHMeYOwrzDSA8kjpLtmDLEWovFPIu0130_assertion SIO_000772 10391218 NP164070.RARKtHbvtU6LZguEHMeYOwrzDSA8kjpLtmDLEWovFPIu0130_provenance.
- NP164070.RARKtHbvtU6LZguEHMeYOwrzDSA8kjpLtmDLEWovFPIu0130_assertion wasDerivedFrom befree-20140225 NP164070.RARKtHbvtU6LZguEHMeYOwrzDSA8kjpLtmDLEWovFPIu0130_provenance.
- NP164070.RARKtHbvtU6LZguEHMeYOwrzDSA8kjpLtmDLEWovFPIu0130_assertion wasGeneratedBy ECO_0000203 NP164070.RARKtHbvtU6LZguEHMeYOwrzDSA8kjpLtmDLEWovFPIu0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP164070.RARKtHbvtU6LZguEHMeYOwrzDSA8kjpLtmDLEWovFPIu0130_provenance.