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- source_evidence_literature type ECO_0000212 NP768958.RAB9PHngpeUO4Ns5WU98UBV1xnpyF70ZTg_w0dP-vwVLc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768958.RAB9PHngpeUO4Ns5WU98UBV1xnpyF70ZTg_w0dP-vwVLc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768958.RAB9PHngpeUO4Ns5WU98UBV1xnpyF70ZTg_w0dP-vwVLc130_provenance.
- NP768958.RAB9PHngpeUO4Ns5WU98UBV1xnpyF70ZTg_w0dP-vwVLc130_assertion description "[Mutations of the valosin-containing protein gene (VCP) are responsible for autosomal-dominant hereditary inclusion-body myopathy associated with frontotemporal dementia and Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768958.RAB9PHngpeUO4Ns5WU98UBV1xnpyF70ZTg_w0dP-vwVLc130_provenance.
- NP768958.RAB9PHngpeUO4Ns5WU98UBV1xnpyF70ZTg_w0dP-vwVLc130_assertion evidence source_evidence_literature NP768958.RAB9PHngpeUO4Ns5WU98UBV1xnpyF70ZTg_w0dP-vwVLc130_provenance.
- NP768958.RAB9PHngpeUO4Ns5WU98UBV1xnpyF70ZTg_w0dP-vwVLc130_assertion SIO_000772 17763460 NP768958.RAB9PHngpeUO4Ns5WU98UBV1xnpyF70ZTg_w0dP-vwVLc130_provenance.
- NP768958.RAB9PHngpeUO4Ns5WU98UBV1xnpyF70ZTg_w0dP-vwVLc130_assertion wasDerivedFrom befree-20150227 NP768958.RAB9PHngpeUO4Ns5WU98UBV1xnpyF70ZTg_w0dP-vwVLc130_provenance.
- NP768958.RAB9PHngpeUO4Ns5WU98UBV1xnpyF70ZTg_w0dP-vwVLc130_assertion wasGeneratedBy ECO_0000203 NP768958.RAB9PHngpeUO4Ns5WU98UBV1xnpyF70ZTg_w0dP-vwVLc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP768958.RAB9PHngpeUO4Ns5WU98UBV1xnpyF70ZTg_w0dP-vwVLc130_provenance.