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- source_evidence_literature type ECO_0000212 NP1242239.RABA5ZhdpKCwUshBJPfbz_jw9ZEfAqNjGkuNfVZ2sWLNU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1242239.RABA5ZhdpKCwUshBJPfbz_jw9ZEfAqNjGkuNfVZ2sWLNU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1242239.RABA5ZhdpKCwUshBJPfbz_jw9ZEfAqNjGkuNfVZ2sWLNU130_provenance.
- NP1242239.RABA5ZhdpKCwUshBJPfbz_jw9ZEfAqNjGkuNfVZ2sWLNU130_assertion description "[A genetic deficiency of VCP can cause inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242239.RABA5ZhdpKCwUshBJPfbz_jw9ZEfAqNjGkuNfVZ2sWLNU130_provenance.
- NP1242239.RABA5ZhdpKCwUshBJPfbz_jw9ZEfAqNjGkuNfVZ2sWLNU130_assertion evidence source_evidence_literature NP1242239.RABA5ZhdpKCwUshBJPfbz_jw9ZEfAqNjGkuNfVZ2sWLNU130_provenance.
- NP1242239.RABA5ZhdpKCwUshBJPfbz_jw9ZEfAqNjGkuNfVZ2sWLNU130_assertion SIO_000772 25447673 NP1242239.RABA5ZhdpKCwUshBJPfbz_jw9ZEfAqNjGkuNfVZ2sWLNU130_provenance.
- NP1242239.RABA5ZhdpKCwUshBJPfbz_jw9ZEfAqNjGkuNfVZ2sWLNU130_assertion wasDerivedFrom befree-2016 NP1242239.RABA5ZhdpKCwUshBJPfbz_jw9ZEfAqNjGkuNfVZ2sWLNU130_provenance.
- NP1242239.RABA5ZhdpKCwUshBJPfbz_jw9ZEfAqNjGkuNfVZ2sWLNU130_assertion wasGeneratedBy ECO_0000203 NP1242239.RABA5ZhdpKCwUshBJPfbz_jw9ZEfAqNjGkuNfVZ2sWLNU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1242239.RABA5ZhdpKCwUshBJPfbz_jw9ZEfAqNjGkuNfVZ2sWLNU130_provenance.