Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP320361.RAI_eDclZuMbk-awNmrBXjejfkBxQc72o5L48eGsA1xdA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP320361.RAI_eDclZuMbk-awNmrBXjejfkBxQc72o5L48eGsA1xdA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP320361.RAI_eDclZuMbk-awNmrBXjejfkBxQc72o5L48eGsA1xdA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP320361.RAI_eDclZuMbk-awNmrBXjejfkBxQc72o5L48eGsA1xdA130_provenance.
- NP320361.RAI_eDclZuMbk-awNmrBXjejfkBxQc72o5L48eGsA1xdA130_assertion description "[This familial case has the characteristic features of myosclerosis myopathy and carries a homozygous COL6A2 mutation responsible for a peculiar pattern of collagen VI defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320361.RAI_eDclZuMbk-awNmrBXjejfkBxQc72o5L48eGsA1xdA130_provenance.
- NP320361.RAI_eDclZuMbk-awNmrBXjejfkBxQc72o5L48eGsA1xdA130_assertion evidence source_evidence_literature NP320361.RAI_eDclZuMbk-awNmrBXjejfkBxQc72o5L48eGsA1xdA130_provenance.
- NP320361.RAI_eDclZuMbk-awNmrBXjejfkBxQc72o5L48eGsA1xdA130_assertion SIO_000772 18852439 NP320361.RAI_eDclZuMbk-awNmrBXjejfkBxQc72o5L48eGsA1xdA130_provenance.
- NP320361.RAI_eDclZuMbk-awNmrBXjejfkBxQc72o5L48eGsA1xdA130_assertion wasDerivedFrom befree-20150227 NP320361.RAI_eDclZuMbk-awNmrBXjejfkBxQc72o5L48eGsA1xdA130_provenance.
- NP320361.RAI_eDclZuMbk-awNmrBXjejfkBxQc72o5L48eGsA1xdA130_assertion wasGeneratedBy ECO_0000203 NP320361.RAI_eDclZuMbk-awNmrBXjejfkBxQc72o5L48eGsA1xdA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP320361.RAI_eDclZuMbk-awNmrBXjejfkBxQc72o5L48eGsA1xdA130_provenance.