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- source_evidence_literature type ECO_0000212 NP978111.RA6AqWfNo-F9CetQoawGlemy31lf_nCQWD6rZT-u0ZM7g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978111.RA6AqWfNo-F9CetQoawGlemy31lf_nCQWD6rZT-u0ZM7g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978111.RA6AqWfNo-F9CetQoawGlemy31lf_nCQWD6rZT-u0ZM7g130_provenance.
- NP978111.RA6AqWfNo-F9CetQoawGlemy31lf_nCQWD6rZT-u0ZM7g130_assertion description "[One of those genes is Aristaless related homeobox (ARX) encoding a polyA-rich homeobox transcription factor essential for cerebral patterning and its mutations cause different neurologic disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978111.RA6AqWfNo-F9CetQoawGlemy31lf_nCQWD6rZT-u0ZM7g130_provenance.
- NP978111.RA6AqWfNo-F9CetQoawGlemy31lf_nCQWD6rZT-u0ZM7g130_assertion evidence source_evidence_literature NP978111.RA6AqWfNo-F9CetQoawGlemy31lf_nCQWD6rZT-u0ZM7g130_provenance.
- NP978111.RA6AqWfNo-F9CetQoawGlemy31lf_nCQWD6rZT-u0ZM7g130_assertion SIO_000772 17480217 NP978111.RA6AqWfNo-F9CetQoawGlemy31lf_nCQWD6rZT-u0ZM7g130_provenance.
- NP978111.RA6AqWfNo-F9CetQoawGlemy31lf_nCQWD6rZT-u0ZM7g130_assertion wasDerivedFrom befree-20150227 NP978111.RA6AqWfNo-F9CetQoawGlemy31lf_nCQWD6rZT-u0ZM7g130_provenance.
- NP978111.RA6AqWfNo-F9CetQoawGlemy31lf_nCQWD6rZT-u0ZM7g130_assertion wasGeneratedBy ECO_0000203 NP978111.RA6AqWfNo-F9CetQoawGlemy31lf_nCQWD6rZT-u0ZM7g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978111.RA6AqWfNo-F9CetQoawGlemy31lf_nCQWD6rZT-u0ZM7g130_provenance.