Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP319268.RATAT5HMgQ4MzWgZwGJ1TWmOKHuw8BWgjAvSGVoJwl5HU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP319268.RATAT5HMgQ4MzWgZwGJ1TWmOKHuw8BWgjAvSGVoJwl5HU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP319268.RATAT5HMgQ4MzWgZwGJ1TWmOKHuw8BWgjAvSGVoJwl5HU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP319268.RATAT5HMgQ4MzWgZwGJ1TWmOKHuw8BWgjAvSGVoJwl5HU130_provenance.
- NP319268.RATAT5HMgQ4MzWgZwGJ1TWmOKHuw8BWgjAvSGVoJwl5HU130_assertion description "[The conclusion that most variants of OI are caused by mutations in the structural genes for type I procollagen has broad implications for other diseases that affect connective tissue, diseases such as chondrodystrophies, osteoarthritis, and osteoporosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319268.RATAT5HMgQ4MzWgZwGJ1TWmOKHuw8BWgjAvSGVoJwl5HU130_provenance.
- NP319268.RATAT5HMgQ4MzWgZwGJ1TWmOKHuw8BWgjAvSGVoJwl5HU130_assertion evidence source_evidence_literature NP319268.RATAT5HMgQ4MzWgZwGJ1TWmOKHuw8BWgjAvSGVoJwl5HU130_provenance.
- NP319268.RATAT5HMgQ4MzWgZwGJ1TWmOKHuw8BWgjAvSGVoJwl5HU130_assertion SIO_000772 2683782 NP319268.RATAT5HMgQ4MzWgZwGJ1TWmOKHuw8BWgjAvSGVoJwl5HU130_provenance.
- NP319268.RATAT5HMgQ4MzWgZwGJ1TWmOKHuw8BWgjAvSGVoJwl5HU130_assertion wasDerivedFrom befree-20150227 NP319268.RATAT5HMgQ4MzWgZwGJ1TWmOKHuw8BWgjAvSGVoJwl5HU130_provenance.
- NP319268.RATAT5HMgQ4MzWgZwGJ1TWmOKHuw8BWgjAvSGVoJwl5HU130_assertion wasGeneratedBy ECO_0000203 NP319268.RATAT5HMgQ4MzWgZwGJ1TWmOKHuw8BWgjAvSGVoJwl5HU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP319268.RATAT5HMgQ4MzWgZwGJ1TWmOKHuw8BWgjAvSGVoJwl5HU130_provenance.