Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP320804.RAngVf39JH2UtF3rzbQD_v3QCLBtO5BQ2MlQH9I_6yF-g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP320804.RAngVf39JH2UtF3rzbQD_v3QCLBtO5BQ2MlQH9I_6yF-g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP320804.RAngVf39JH2UtF3rzbQD_v3QCLBtO5BQ2MlQH9I_6yF-g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP320804.RAngVf39JH2UtF3rzbQD_v3QCLBtO5BQ2MlQH9I_6yF-g130_provenance.
- NP320804.RAngVf39JH2UtF3rzbQD_v3QCLBtO5BQ2MlQH9I_6yF-g130_assertion description "[The cloning of bovine and then human collagen type X genes facilitated studies in relevant human diseases and contributed to the discovery of mutations in the COL10A1 gene in families with metaphyseal chondrodysplasia type Schmid.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320804.RAngVf39JH2UtF3rzbQD_v3QCLBtO5BQ2MlQH9I_6yF-g130_provenance.
- NP320804.RAngVf39JH2UtF3rzbQD_v3QCLBtO5BQ2MlQH9I_6yF-g130_assertion evidence source_evidence_literature NP320804.RAngVf39JH2UtF3rzbQD_v3QCLBtO5BQ2MlQH9I_6yF-g130_provenance.
- NP320804.RAngVf39JH2UtF3rzbQD_v3QCLBtO5BQ2MlQH9I_6yF-g130_assertion SIO_000772 17696900 NP320804.RAngVf39JH2UtF3rzbQD_v3QCLBtO5BQ2MlQH9I_6yF-g130_provenance.
- NP320804.RAngVf39JH2UtF3rzbQD_v3QCLBtO5BQ2MlQH9I_6yF-g130_assertion wasDerivedFrom befree-20150227 NP320804.RAngVf39JH2UtF3rzbQD_v3QCLBtO5BQ2MlQH9I_6yF-g130_provenance.
- NP320804.RAngVf39JH2UtF3rzbQD_v3QCLBtO5BQ2MlQH9I_6yF-g130_assertion wasGeneratedBy ECO_0000203 NP320804.RAngVf39JH2UtF3rzbQD_v3QCLBtO5BQ2MlQH9I_6yF-g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP320804.RAngVf39JH2UtF3rzbQD_v3QCLBtO5BQ2MlQH9I_6yF-g130_provenance.