Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP178233.RAB8OKfVjlSigPhLaH4UlM2jghqRK2n9h0cNEaBj_kWAw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP178233.RAB8OKfVjlSigPhLaH4UlM2jghqRK2n9h0cNEaBj_kWAw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP178233.RAB8OKfVjlSigPhLaH4UlM2jghqRK2n9h0cNEaBj_kWAw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP178233.RAB8OKfVjlSigPhLaH4UlM2jghqRK2n9h0cNEaBj_kWAw130_provenance.
- NP178233.RAB8OKfVjlSigPhLaH4UlM2jghqRK2n9h0cNEaBj_kWAw130_assertion description "[Charcot-Marie-Tooth neuropathy type 1 (CMT1) is a genetically heterogeneous group of chronic demyelinating polyneuropathies with loci mapping to chromosome 17p (CMT1A), chromosome 1q (CMT1B), the X chromosome (CMTX) and to another unknown autosome (CMT1C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178233.RAB8OKfVjlSigPhLaH4UlM2jghqRK2n9h0cNEaBj_kWAw130_provenance.
- NP178233.RAB8OKfVjlSigPhLaH4UlM2jghqRK2n9h0cNEaBj_kWAw130_assertion evidence source_evidence_literature NP178233.RAB8OKfVjlSigPhLaH4UlM2jghqRK2n9h0cNEaBj_kWAw130_provenance.
- NP178233.RAB8OKfVjlSigPhLaH4UlM2jghqRK2n9h0cNEaBj_kWAw130_assertion SIO_000772 7952853 NP178233.RAB8OKfVjlSigPhLaH4UlM2jghqRK2n9h0cNEaBj_kWAw130_provenance.
- NP178233.RAB8OKfVjlSigPhLaH4UlM2jghqRK2n9h0cNEaBj_kWAw130_assertion wasDerivedFrom befree-20140225 NP178233.RAB8OKfVjlSigPhLaH4UlM2jghqRK2n9h0cNEaBj_kWAw130_provenance.
- NP178233.RAB8OKfVjlSigPhLaH4UlM2jghqRK2n9h0cNEaBj_kWAw130_assertion wasGeneratedBy ECO_0000203 NP178233.RAB8OKfVjlSigPhLaH4UlM2jghqRK2n9h0cNEaBj_kWAw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP178233.RAB8OKfVjlSigPhLaH4UlM2jghqRK2n9h0cNEaBj_kWAw130_provenance.