Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP368878.RApDoT-cHjCm_lHf8Lea5-jgDfulQap7JY7Dl1xOpixAE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP368878.RApDoT-cHjCm_lHf8Lea5-jgDfulQap7JY7Dl1xOpixAE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP368878.RApDoT-cHjCm_lHf8Lea5-jgDfulQap7JY7Dl1xOpixAE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP368878.RApDoT-cHjCm_lHf8Lea5-jgDfulQap7JY7Dl1xOpixAE130_provenance.
- NP368878.RApDoT-cHjCm_lHf8Lea5-jgDfulQap7JY7Dl1xOpixAE130_assertion description "[High throughput mutation screening of the factor VIII gene (F8C) in hemophilia A: 37 novel mutations and genotype-phenotype correlation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP368878.RApDoT-cHjCm_lHf8Lea5-jgDfulQap7JY7Dl1xOpixAE130_provenance.
- NP368878.RApDoT-cHjCm_lHf8Lea5-jgDfulQap7JY7Dl1xOpixAE130_assertion evidence source_evidence_literature NP368878.RApDoT-cHjCm_lHf8Lea5-jgDfulQap7JY7Dl1xOpixAE130_provenance.
- NP368878.RApDoT-cHjCm_lHf8Lea5-jgDfulQap7JY7Dl1xOpixAE130_assertion SIO_000772 12325022 NP368878.RApDoT-cHjCm_lHf8Lea5-jgDfulQap7JY7Dl1xOpixAE130_provenance.
- NP368878.RApDoT-cHjCm_lHf8Lea5-jgDfulQap7JY7Dl1xOpixAE130_assertion wasDerivedFrom befree-2016 NP368878.RApDoT-cHjCm_lHf8Lea5-jgDfulQap7JY7Dl1xOpixAE130_provenance.
- NP368878.RApDoT-cHjCm_lHf8Lea5-jgDfulQap7JY7Dl1xOpixAE130_assertion wasGeneratedBy ECO_0000203 NP368878.RApDoT-cHjCm_lHf8Lea5-jgDfulQap7JY7Dl1xOpixAE130_provenance.
- befree-2016 importedOn "2016-02-19" NP368878.RApDoT-cHjCm_lHf8Lea5-jgDfulQap7JY7Dl1xOpixAE130_provenance.