Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP776573.RAos-_Po0QU5ZeRFf_GZEn76Zy0oMlTnGaQO81f59AGzQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP776573.RAos-_Po0QU5ZeRFf_GZEn76Zy0oMlTnGaQO81f59AGzQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP776573.RAos-_Po0QU5ZeRFf_GZEn76Zy0oMlTnGaQO81f59AGzQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP776573.RAos-_Po0QU5ZeRFf_GZEn76Zy0oMlTnGaQO81f59AGzQ130_provenance.
- NP776573.RAos-_Po0QU5ZeRFf_GZEn76Zy0oMlTnGaQO81f59AGzQ130_assertion description "[In addition, he has vertebral anomalies, brachymelia of the arms, and a ventricular septal defect-features that are reminiscent of Robinow syndrome, which has also been shown to be caused by mutations in ROR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776573.RAos-_Po0QU5ZeRFf_GZEn76Zy0oMlTnGaQO81f59AGzQ130_provenance.
- NP776573.RAos-_Po0QU5ZeRFf_GZEn76Zy0oMlTnGaQO81f59AGzQ130_assertion evidence source_evidence_literature NP776573.RAos-_Po0QU5ZeRFf_GZEn76Zy0oMlTnGaQO81f59AGzQ130_provenance.
- NP776573.RAos-_Po0QU5ZeRFf_GZEn76Zy0oMlTnGaQO81f59AGzQ130_assertion SIO_000772 10986040 NP776573.RAos-_Po0QU5ZeRFf_GZEn76Zy0oMlTnGaQO81f59AGzQ130_provenance.
- NP776573.RAos-_Po0QU5ZeRFf_GZEn76Zy0oMlTnGaQO81f59AGzQ130_assertion wasDerivedFrom befree-20140225 NP776573.RAos-_Po0QU5ZeRFf_GZEn76Zy0oMlTnGaQO81f59AGzQ130_provenance.
- NP776573.RAos-_Po0QU5ZeRFf_GZEn76Zy0oMlTnGaQO81f59AGzQ130_assertion wasGeneratedBy ECO_0000203 NP776573.RAos-_Po0QU5ZeRFf_GZEn76Zy0oMlTnGaQO81f59AGzQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP776573.RAos-_Po0QU5ZeRFf_GZEn76Zy0oMlTnGaQO81f59AGzQ130_provenance.