Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP925347.RAss7Xjzg-3uxaSECyyr2dhF_pk_-AkG39GOyXltydQI0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925347.RAss7Xjzg-3uxaSECyyr2dhF_pk_-AkG39GOyXltydQI0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925347.RAss7Xjzg-3uxaSECyyr2dhF_pk_-AkG39GOyXltydQI0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925347.RAss7Xjzg-3uxaSECyyr2dhF_pk_-AkG39GOyXltydQI0130_provenance.
- NP925347.RAss7Xjzg-3uxaSECyyr2dhF_pk_-AkG39GOyXltydQI0130_assertion description "[A total of 45 unrelated patients with GT were enrolled in the present study to identify the causative molecular defects, and also to correlate their phenotype with their genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925347.RAss7Xjzg-3uxaSECyyr2dhF_pk_-AkG39GOyXltydQI0130_provenance.
- NP925347.RAss7Xjzg-3uxaSECyyr2dhF_pk_-AkG39GOyXltydQI0130_assertion evidence source_evidence_literature NP925347.RAss7Xjzg-3uxaSECyyr2dhF_pk_-AkG39GOyXltydQI0130_provenance.
- NP925347.RAss7Xjzg-3uxaSECyyr2dhF_pk_-AkG39GOyXltydQI0130_assertion SIO_000772 19691478 NP925347.RAss7Xjzg-3uxaSECyyr2dhF_pk_-AkG39GOyXltydQI0130_provenance.
- NP925347.RAss7Xjzg-3uxaSECyyr2dhF_pk_-AkG39GOyXltydQI0130_assertion wasDerivedFrom befree-20150227 NP925347.RAss7Xjzg-3uxaSECyyr2dhF_pk_-AkG39GOyXltydQI0130_provenance.
- NP925347.RAss7Xjzg-3uxaSECyyr2dhF_pk_-AkG39GOyXltydQI0130_assertion wasGeneratedBy ECO_0000203 NP925347.RAss7Xjzg-3uxaSECyyr2dhF_pk_-AkG39GOyXltydQI0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP925347.RAss7Xjzg-3uxaSECyyr2dhF_pk_-AkG39GOyXltydQI0130_provenance.