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- source_evidence_literature type ECO_0000212 NP674256.RAIgTIDDoI0zJiOEJ3ybbjBNQnlNwx2R4ezP3mzK277uk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674256.RAIgTIDDoI0zJiOEJ3ybbjBNQnlNwx2R4ezP3mzK277uk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674256.RAIgTIDDoI0zJiOEJ3ybbjBNQnlNwx2R4ezP3mzK277uk130_provenance.
- NP674256.RAIgTIDDoI0zJiOEJ3ybbjBNQnlNwx2R4ezP3mzK277uk130_assertion description "[Autosomal recessive Robinow syndrome is caused by mutations in ROR2 and is characterized by short stature, mesomelic limb shortening, brachydactyly, vertebral abnormalities, and a characteristic 'fetal face' dysmorphology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674256.RAIgTIDDoI0zJiOEJ3ybbjBNQnlNwx2R4ezP3mzK277uk130_provenance.
- NP674256.RAIgTIDDoI0zJiOEJ3ybbjBNQnlNwx2R4ezP3mzK277uk130_assertion evidence source_evidence_literature NP674256.RAIgTIDDoI0zJiOEJ3ybbjBNQnlNwx2R4ezP3mzK277uk130_provenance.
- NP674256.RAIgTIDDoI0zJiOEJ3ybbjBNQnlNwx2R4ezP3mzK277uk130_assertion SIO_000772 15952209 NP674256.RAIgTIDDoI0zJiOEJ3ybbjBNQnlNwx2R4ezP3mzK277uk130_provenance.
- NP674256.RAIgTIDDoI0zJiOEJ3ybbjBNQnlNwx2R4ezP3mzK277uk130_assertion wasDerivedFrom befree-20150227 NP674256.RAIgTIDDoI0zJiOEJ3ybbjBNQnlNwx2R4ezP3mzK277uk130_provenance.
- NP674256.RAIgTIDDoI0zJiOEJ3ybbjBNQnlNwx2R4ezP3mzK277uk130_assertion wasGeneratedBy ECO_0000203 NP674256.RAIgTIDDoI0zJiOEJ3ybbjBNQnlNwx2R4ezP3mzK277uk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP674256.RAIgTIDDoI0zJiOEJ3ybbjBNQnlNwx2R4ezP3mzK277uk130_provenance.