Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP933354.RAUAZcJ7Rjxb3pCQxT4-v-1pIEvINrDVpgLlbkRsb1EhE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP933354.RAUAZcJ7Rjxb3pCQxT4-v-1pIEvINrDVpgLlbkRsb1EhE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP933354.RAUAZcJ7Rjxb3pCQxT4-v-1pIEvINrDVpgLlbkRsb1EhE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP933354.RAUAZcJ7Rjxb3pCQxT4-v-1pIEvINrDVpgLlbkRsb1EhE130_provenance.
- NP933354.RAUAZcJ7Rjxb3pCQxT4-v-1pIEvINrDVpgLlbkRsb1EhE130_assertion description "[A genetic defect is evident in some cases; known genetic changes include: multiple endocrine neoplasia type 1 (MEN1); Carney complex; McCune-Albright syndrome; and, more recently identified, aryl hydrocarbon receptor-interacting protein (AIP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP933354.RAUAZcJ7Rjxb3pCQxT4-v-1pIEvINrDVpgLlbkRsb1EhE130_provenance.
- NP933354.RAUAZcJ7Rjxb3pCQxT4-v-1pIEvINrDVpgLlbkRsb1EhE130_assertion evidence source_evidence_literature NP933354.RAUAZcJ7Rjxb3pCQxT4-v-1pIEvINrDVpgLlbkRsb1EhE130_provenance.
- NP933354.RAUAZcJ7Rjxb3pCQxT4-v-1pIEvINrDVpgLlbkRsb1EhE130_assertion SIO_000772 22024364 NP933354.RAUAZcJ7Rjxb3pCQxT4-v-1pIEvINrDVpgLlbkRsb1EhE130_provenance.
- NP933354.RAUAZcJ7Rjxb3pCQxT4-v-1pIEvINrDVpgLlbkRsb1EhE130_assertion wasDerivedFrom befree-2016 NP933354.RAUAZcJ7Rjxb3pCQxT4-v-1pIEvINrDVpgLlbkRsb1EhE130_provenance.
- NP933354.RAUAZcJ7Rjxb3pCQxT4-v-1pIEvINrDVpgLlbkRsb1EhE130_assertion wasGeneratedBy ECO_0000203 NP933354.RAUAZcJ7Rjxb3pCQxT4-v-1pIEvINrDVpgLlbkRsb1EhE130_provenance.
- befree-2016 importedOn "2016-02-19" NP933354.RAUAZcJ7Rjxb3pCQxT4-v-1pIEvINrDVpgLlbkRsb1EhE130_provenance.