Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP755535.RA5fHGx6a8ccaBk6nf8NKIAiAdCr1eTGQC3VhbPCQZULE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP755535.RA5fHGx6a8ccaBk6nf8NKIAiAdCr1eTGQC3VhbPCQZULE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP755535.RA5fHGx6a8ccaBk6nf8NKIAiAdCr1eTGQC3VhbPCQZULE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP755535.RA5fHGx6a8ccaBk6nf8NKIAiAdCr1eTGQC3VhbPCQZULE130_provenance.
- NP755535.RA5fHGx6a8ccaBk6nf8NKIAiAdCr1eTGQC3VhbPCQZULE130_assertion description "[Limb-girdle muscular dystrophy type 1D (LGMD1D) was linked to chromosome 7q36 over a decade ago, but its genetic cause has remained elusive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755535.RA5fHGx6a8ccaBk6nf8NKIAiAdCr1eTGQC3VhbPCQZULE130_provenance.
- NP755535.RA5fHGx6a8ccaBk6nf8NKIAiAdCr1eTGQC3VhbPCQZULE130_assertion evidence source_evidence_literature NP755535.RA5fHGx6a8ccaBk6nf8NKIAiAdCr1eTGQC3VhbPCQZULE130_provenance.
- NP755535.RA5fHGx6a8ccaBk6nf8NKIAiAdCr1eTGQC3VhbPCQZULE130_assertion SIO_000772 22366786 NP755535.RA5fHGx6a8ccaBk6nf8NKIAiAdCr1eTGQC3VhbPCQZULE130_provenance.
- NP755535.RA5fHGx6a8ccaBk6nf8NKIAiAdCr1eTGQC3VhbPCQZULE130_assertion wasDerivedFrom befree-20140225 NP755535.RA5fHGx6a8ccaBk6nf8NKIAiAdCr1eTGQC3VhbPCQZULE130_provenance.
- NP755535.RA5fHGx6a8ccaBk6nf8NKIAiAdCr1eTGQC3VhbPCQZULE130_assertion wasGeneratedBy ECO_0000203 NP755535.RA5fHGx6a8ccaBk6nf8NKIAiAdCr1eTGQC3VhbPCQZULE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP755535.RA5fHGx6a8ccaBk6nf8NKIAiAdCr1eTGQC3VhbPCQZULE130_provenance.