Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP377592.RAOhdaTNv8aaLlUfqbe9RNVbSZgMPmepqB1qLPXDZtzQw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP377592.RAOhdaTNv8aaLlUfqbe9RNVbSZgMPmepqB1qLPXDZtzQw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP377592.RAOhdaTNv8aaLlUfqbe9RNVbSZgMPmepqB1qLPXDZtzQw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP377592.RAOhdaTNv8aaLlUfqbe9RNVbSZgMPmepqB1qLPXDZtzQw130_provenance.
- NP377592.RAOhdaTNv8aaLlUfqbe9RNVbSZgMPmepqB1qLPXDZtzQw130_assertion description "[We analysed the DNA of one family with hereditary glomuvenous malformations and identified the mutation causing the disease in the glomulin gene on chromosome 1 p22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP377592.RAOhdaTNv8aaLlUfqbe9RNVbSZgMPmepqB1qLPXDZtzQw130_provenance.
- NP377592.RAOhdaTNv8aaLlUfqbe9RNVbSZgMPmepqB1qLPXDZtzQw130_assertion evidence source_evidence_literature NP377592.RAOhdaTNv8aaLlUfqbe9RNVbSZgMPmepqB1qLPXDZtzQw130_provenance.
- NP377592.RAOhdaTNv8aaLlUfqbe9RNVbSZgMPmepqB1qLPXDZtzQw130_assertion SIO_000772 17680968 NP377592.RAOhdaTNv8aaLlUfqbe9RNVbSZgMPmepqB1qLPXDZtzQw130_provenance.
- NP377592.RAOhdaTNv8aaLlUfqbe9RNVbSZgMPmepqB1qLPXDZtzQw130_assertion wasDerivedFrom befree-20140225 NP377592.RAOhdaTNv8aaLlUfqbe9RNVbSZgMPmepqB1qLPXDZtzQw130_provenance.
- NP377592.RAOhdaTNv8aaLlUfqbe9RNVbSZgMPmepqB1qLPXDZtzQw130_assertion wasGeneratedBy ECO_0000203 NP377592.RAOhdaTNv8aaLlUfqbe9RNVbSZgMPmepqB1qLPXDZtzQw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP377592.RAOhdaTNv8aaLlUfqbe9RNVbSZgMPmepqB1qLPXDZtzQw130_provenance.