Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP693498.RA6i2zKXUSPgzixO18xleT9amNbAVZpwIBCLqkb67C0a8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP693498.RA6i2zKXUSPgzixO18xleT9amNbAVZpwIBCLqkb67C0a8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP693498.RA6i2zKXUSPgzixO18xleT9amNbAVZpwIBCLqkb67C0a8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP693498.RA6i2zKXUSPgzixO18xleT9amNbAVZpwIBCLqkb67C0a8130_provenance.
- NP693498.RA6i2zKXUSPgzixO18xleT9amNbAVZpwIBCLqkb67C0a8130_assertion description "[Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency..]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693498.RA6i2zKXUSPgzixO18xleT9amNbAVZpwIBCLqkb67C0a8130_provenance.
- NP693498.RA6i2zKXUSPgzixO18xleT9amNbAVZpwIBCLqkb67C0a8130_assertion evidence source_evidence_literature NP693498.RA6i2zKXUSPgzixO18xleT9amNbAVZpwIBCLqkb67C0a8130_provenance.
- NP693498.RA6i2zKXUSPgzixO18xleT9amNbAVZpwIBCLqkb67C0a8130_assertion SIO_000772 10852374 NP693498.RA6i2zKXUSPgzixO18xleT9amNbAVZpwIBCLqkb67C0a8130_provenance.
- NP693498.RA6i2zKXUSPgzixO18xleT9amNbAVZpwIBCLqkb67C0a8130_assertion wasDerivedFrom befree-20150227 NP693498.RA6i2zKXUSPgzixO18xleT9amNbAVZpwIBCLqkb67C0a8130_provenance.
- NP693498.RA6i2zKXUSPgzixO18xleT9amNbAVZpwIBCLqkb67C0a8130_assertion wasGeneratedBy ECO_0000203 NP693498.RA6i2zKXUSPgzixO18xleT9amNbAVZpwIBCLqkb67C0a8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP693498.RA6i2zKXUSPgzixO18xleT9amNbAVZpwIBCLqkb67C0a8130_provenance.