Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP777010.RANHupM0VXvXjc3DH5dzJ9GmxMQP9Ef6nlt2fdxeGNS8Y130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP777010.RANHupM0VXvXjc3DH5dzJ9GmxMQP9Ef6nlt2fdxeGNS8Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP777010.RANHupM0VXvXjc3DH5dzJ9GmxMQP9Ef6nlt2fdxeGNS8Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP777010.RANHupM0VXvXjc3DH5dzJ9GmxMQP9Ef6nlt2fdxeGNS8Y130_provenance.
- NP777010.RANHupM0VXvXjc3DH5dzJ9GmxMQP9Ef6nlt2fdxeGNS8Y130_assertion description "[We describe the results of prenatal analyses and postnatal findings in a male fetus with a partial trisomy for the long arm and a small terminal monosomy for the short arm of chromosome 4 with the following karyotype: 46,XY,add(4)(p16.3).ish dup(4)(q26qter)(wcp4+, D4S2336x3,AFMb280xa5x2,4ptel-,WHCR-).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP777010.RANHupM0VXvXjc3DH5dzJ9GmxMQP9Ef6nlt2fdxeGNS8Y130_provenance.
- NP777010.RANHupM0VXvXjc3DH5dzJ9GmxMQP9Ef6nlt2fdxeGNS8Y130_assertion evidence source_evidence_literature NP777010.RANHupM0VXvXjc3DH5dzJ9GmxMQP9Ef6nlt2fdxeGNS8Y130_provenance.
- NP777010.RANHupM0VXvXjc3DH5dzJ9GmxMQP9Ef6nlt2fdxeGNS8Y130_assertion SIO_000772 10740212 NP777010.RANHupM0VXvXjc3DH5dzJ9GmxMQP9Ef6nlt2fdxeGNS8Y130_provenance.
- NP777010.RANHupM0VXvXjc3DH5dzJ9GmxMQP9Ef6nlt2fdxeGNS8Y130_assertion wasDerivedFrom befree-20150227 NP777010.RANHupM0VXvXjc3DH5dzJ9GmxMQP9Ef6nlt2fdxeGNS8Y130_provenance.
- NP777010.RANHupM0VXvXjc3DH5dzJ9GmxMQP9Ef6nlt2fdxeGNS8Y130_assertion wasGeneratedBy ECO_0000203 NP777010.RANHupM0VXvXjc3DH5dzJ9GmxMQP9Ef6nlt2fdxeGNS8Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP777010.RANHupM0VXvXjc3DH5dzJ9GmxMQP9Ef6nlt2fdxeGNS8Y130_provenance.