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- source_evidence_literature type ECO_0000212 NP827274.RA99_7VQ0TFCF1DWH8nyXFexip_AstDxH9hyHMYai2yEU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP827274.RA99_7VQ0TFCF1DWH8nyXFexip_AstDxH9hyHMYai2yEU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP827274.RA99_7VQ0TFCF1DWH8nyXFexip_AstDxH9hyHMYai2yEU130_provenance.
- NP827274.RA99_7VQ0TFCF1DWH8nyXFexip_AstDxH9hyHMYai2yEU130_assertion description "[Charcot-Marie-Tooth disease comprises a heterogeneous group of hereditary neuropathies which fall into two main groups: demyelinating CMT1 with reduced nerve conduction velocity and axonal CMT2 with normal nerve conduction velocity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP827274.RA99_7VQ0TFCF1DWH8nyXFexip_AstDxH9hyHMYai2yEU130_provenance.
- NP827274.RA99_7VQ0TFCF1DWH8nyXFexip_AstDxH9hyHMYai2yEU130_assertion evidence source_evidence_literature NP827274.RA99_7VQ0TFCF1DWH8nyXFexip_AstDxH9hyHMYai2yEU130_provenance.
- NP827274.RA99_7VQ0TFCF1DWH8nyXFexip_AstDxH9hyHMYai2yEU130_assertion SIO_000772 14733962 NP827274.RA99_7VQ0TFCF1DWH8nyXFexip_AstDxH9hyHMYai2yEU130_provenance.
- NP827274.RA99_7VQ0TFCF1DWH8nyXFexip_AstDxH9hyHMYai2yEU130_assertion wasDerivedFrom befree-20150227 NP827274.RA99_7VQ0TFCF1DWH8nyXFexip_AstDxH9hyHMYai2yEU130_provenance.
- NP827274.RA99_7VQ0TFCF1DWH8nyXFexip_AstDxH9hyHMYai2yEU130_assertion wasGeneratedBy ECO_0000203 NP827274.RA99_7VQ0TFCF1DWH8nyXFexip_AstDxH9hyHMYai2yEU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP827274.RA99_7VQ0TFCF1DWH8nyXFexip_AstDxH9hyHMYai2yEU130_provenance.