Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP964774.RAwLV_84RqAWZqEKVmtl4dw8Z9FIBI-PR3EFHG2cUzVfY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP964774.RAwLV_84RqAWZqEKVmtl4dw8Z9FIBI-PR3EFHG2cUzVfY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP964774.RAwLV_84RqAWZqEKVmtl4dw8Z9FIBI-PR3EFHG2cUzVfY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP964774.RAwLV_84RqAWZqEKVmtl4dw8Z9FIBI-PR3EFHG2cUzVfY130_provenance.
- NP964774.RAwLV_84RqAWZqEKVmtl4dw8Z9FIBI-PR3EFHG2cUzVfY130_assertion description "[A novel deletion partly removing the AVP gene causes autosomal recessive inheritance of early-onset neurohypophyseal diabetes insipidus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP964774.RAwLV_84RqAWZqEKVmtl4dw8Z9FIBI-PR3EFHG2cUzVfY130_provenance.
- NP964774.RAwLV_84RqAWZqEKVmtl4dw8Z9FIBI-PR3EFHG2cUzVfY130_assertion evidence source_evidence_literature NP964774.RAwLV_84RqAWZqEKVmtl4dw8Z9FIBI-PR3EFHG2cUzVfY130_provenance.
- NP964774.RAwLV_84RqAWZqEKVmtl4dw8Z9FIBI-PR3EFHG2cUzVfY130_assertion SIO_000772 22168581 NP964774.RAwLV_84RqAWZqEKVmtl4dw8Z9FIBI-PR3EFHG2cUzVfY130_provenance.
- NP964774.RAwLV_84RqAWZqEKVmtl4dw8Z9FIBI-PR3EFHG2cUzVfY130_assertion wasDerivedFrom befree-20150227 NP964774.RAwLV_84RqAWZqEKVmtl4dw8Z9FIBI-PR3EFHG2cUzVfY130_provenance.
- NP964774.RAwLV_84RqAWZqEKVmtl4dw8Z9FIBI-PR3EFHG2cUzVfY130_assertion wasGeneratedBy ECO_0000203 NP964774.RAwLV_84RqAWZqEKVmtl4dw8Z9FIBI-PR3EFHG2cUzVfY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP964774.RAwLV_84RqAWZqEKVmtl4dw8Z9FIBI-PR3EFHG2cUzVfY130_provenance.