Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP421359.RADH6OV9YufGlomepa0s4iON7JCw39KwjRI4JdSd5w6lw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP421359.RADH6OV9YufGlomepa0s4iON7JCw39KwjRI4JdSd5w6lw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP421359.RADH6OV9YufGlomepa0s4iON7JCw39KwjRI4JdSd5w6lw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP421359.RADH6OV9YufGlomepa0s4iON7JCw39KwjRI4JdSd5w6lw130_provenance.
- NP421359.RADH6OV9YufGlomepa0s4iON7JCw39KwjRI4JdSd5w6lw130_assertion description "[Germline CDH1 mutations are not always detectable in patients who meet the HDGC criteria and the aetiological role of this gene is still under investigation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP421359.RADH6OV9YufGlomepa0s4iON7JCw39KwjRI4JdSd5w6lw130_provenance.
- NP421359.RADH6OV9YufGlomepa0s4iON7JCw39KwjRI4JdSd5w6lw130_assertion evidence source_evidence_literature NP421359.RADH6OV9YufGlomepa0s4iON7JCw39KwjRI4JdSd5w6lw130_provenance.
- NP421359.RADH6OV9YufGlomepa0s4iON7JCw39KwjRI4JdSd5w6lw130_assertion SIO_000772 14630673 NP421359.RADH6OV9YufGlomepa0s4iON7JCw39KwjRI4JdSd5w6lw130_provenance.
- NP421359.RADH6OV9YufGlomepa0s4iON7JCw39KwjRI4JdSd5w6lw130_assertion wasDerivedFrom befree-2016 NP421359.RADH6OV9YufGlomepa0s4iON7JCw39KwjRI4JdSd5w6lw130_provenance.
- NP421359.RADH6OV9YufGlomepa0s4iON7JCw39KwjRI4JdSd5w6lw130_assertion wasGeneratedBy ECO_0000203 NP421359.RADH6OV9YufGlomepa0s4iON7JCw39KwjRI4JdSd5w6lw130_provenance.
- befree-2016 importedOn "2016-02-19" NP421359.RADH6OV9YufGlomepa0s4iON7JCw39KwjRI4JdSd5w6lw130_provenance.