Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_provenance.
- NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_assertion description "[Mutations in ROR2 have been shown to cause two distinct human disorders, autosomal recessive Robinow syndrome and dominantly inherited Brachydactyly type B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_provenance.
- NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_assertion evidence source_evidence_literature NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_provenance.
- NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_assertion SIO_000772 17665217 NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_provenance.
- NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_assertion wasDerivedFrom befree-20150227 NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_provenance.
- NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_assertion wasGeneratedBy ECO_0000203 NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP600542.RAgbbR3czXSmpmYZxVD6P076ODxKN8pswgNbnKr2EcJ9Y130_provenance.