Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP312211.RAEscUYx2RiNlwyLp6DH2Rjo-GdGKS3ng9YyI1AYRLgvc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP312211.RAEscUYx2RiNlwyLp6DH2Rjo-GdGKS3ng9YyI1AYRLgvc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP312211.RAEscUYx2RiNlwyLp6DH2Rjo-GdGKS3ng9YyI1AYRLgvc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP312211.RAEscUYx2RiNlwyLp6DH2Rjo-GdGKS3ng9YyI1AYRLgvc130_provenance.
- NP312211.RAEscUYx2RiNlwyLp6DH2Rjo-GdGKS3ng9YyI1AYRLgvc130_assertion description "[One form of CMT2 maps to chromosome 1p36 (CMT2A), another to chromosome 3p (CMT2B) and another to 7p (CMT2D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312211.RAEscUYx2RiNlwyLp6DH2Rjo-GdGKS3ng9YyI1AYRLgvc130_provenance.
- NP312211.RAEscUYx2RiNlwyLp6DH2Rjo-GdGKS3ng9YyI1AYRLgvc130_assertion evidence source_evidence_literature NP312211.RAEscUYx2RiNlwyLp6DH2Rjo-GdGKS3ng9YyI1AYRLgvc130_provenance.
- NP312211.RAEscUYx2RiNlwyLp6DH2Rjo-GdGKS3ng9YyI1AYRLgvc130_assertion SIO_000772 10219749 NP312211.RAEscUYx2RiNlwyLp6DH2Rjo-GdGKS3ng9YyI1AYRLgvc130_provenance.
- NP312211.RAEscUYx2RiNlwyLp6DH2Rjo-GdGKS3ng9YyI1AYRLgvc130_assertion wasDerivedFrom befree-20140225 NP312211.RAEscUYx2RiNlwyLp6DH2Rjo-GdGKS3ng9YyI1AYRLgvc130_provenance.
- NP312211.RAEscUYx2RiNlwyLp6DH2Rjo-GdGKS3ng9YyI1AYRLgvc130_assertion wasGeneratedBy ECO_0000203 NP312211.RAEscUYx2RiNlwyLp6DH2Rjo-GdGKS3ng9YyI1AYRLgvc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP312211.RAEscUYx2RiNlwyLp6DH2Rjo-GdGKS3ng9YyI1AYRLgvc130_provenance.