Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP689776.RATT0xO56_bQXYB9M9G-IBhoz9JSdvk9-d47zfTydlkKo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP689776.RATT0xO56_bQXYB9M9G-IBhoz9JSdvk9-d47zfTydlkKo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP689776.RATT0xO56_bQXYB9M9G-IBhoz9JSdvk9-d47zfTydlkKo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP689776.RATT0xO56_bQXYB9M9G-IBhoz9JSdvk9-d47zfTydlkKo130_provenance.
- NP689776.RATT0xO56_bQXYB9M9G-IBhoz9JSdvk9-d47zfTydlkKo130_assertion description "[The sLe(x)-Neg variant of the 4T1 cell line with markedly diminished expression of sLe(x) and lack of sLe(a), provided a unique opportunity to characterize P-selectin ligands and their contribution to metastasis in the absence of overlapping selectin ligands and E-selectin binding.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP689776.RATT0xO56_bQXYB9M9G-IBhoz9JSdvk9-d47zfTydlkKo130_provenance.
- NP689776.RATT0xO56_bQXYB9M9G-IBhoz9JSdvk9-d47zfTydlkKo130_assertion evidence source_evidence_literature NP689776.RATT0xO56_bQXYB9M9G-IBhoz9JSdvk9-d47zfTydlkKo130_provenance.
- NP689776.RATT0xO56_bQXYB9M9G-IBhoz9JSdvk9-d47zfTydlkKo130_assertion SIO_000772 17154173 NP689776.RATT0xO56_bQXYB9M9G-IBhoz9JSdvk9-d47zfTydlkKo130_provenance.
- NP689776.RATT0xO56_bQXYB9M9G-IBhoz9JSdvk9-d47zfTydlkKo130_assertion wasDerivedFrom befree-20150227 NP689776.RATT0xO56_bQXYB9M9G-IBhoz9JSdvk9-d47zfTydlkKo130_provenance.
- NP689776.RATT0xO56_bQXYB9M9G-IBhoz9JSdvk9-d47zfTydlkKo130_assertion wasGeneratedBy ECO_0000203 NP689776.RATT0xO56_bQXYB9M9G-IBhoz9JSdvk9-d47zfTydlkKo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP689776.RATT0xO56_bQXYB9M9G-IBhoz9JSdvk9-d47zfTydlkKo130_provenance.