Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_provenance.
- NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_assertion description "[The common mesenchymal origin of GVM and lymphatic vessels as well as the glomulin expression in vascular smooth muscle cells in utero could help explain this unusual prenatal complication of glomuvenous malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_provenance.
- NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_assertion evidence source_evidence_literature NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_provenance.
- NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_assertion SIO_000772 21510024 NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_provenance.
- NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_assertion wasDerivedFrom befree-20140225 NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_provenance.
- NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_assertion wasGeneratedBy ECO_0000203 NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_provenance.